Attachment A-2 FIFRA Sec 24c

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FEDERAL INSECTICIDE, FUNGICIDE, AND
RODENTICIDE ACT
[As Amended Through P.L. 112–177, Effective Sept. 28, 2012]
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1. [prec. 121] Short title and table of contents.
2. [136] Definitions.
3. [136a] Registration of pesticides.
4. [136a–1] Reregistration of registered pesticides.
5. [136c] Experimental use permits.
6. [136d] Administrative review; suspension.
7. [136e] Registration of establishments.
8. [136f] Books and records.
9. [136g] Inspection of establishments, etc.
10. [136h] Protection of trade secrets and other information.
11. [136i] Use of restricted use pesticides; applicators.
12. [136j] Unlawful acts.
13. [136k] Stop sale, use, removal, and seizure.
14. [136l] Penalties.
15. [136m] Indemnities.
16. [136n] Administrative procedure; judicial review.
17. [136o] Imports and exports.
18. [136p] Exemption of Federal and State agencies.
19. [136q] Storage, disposal, transportation, and recall.
20. [136r] Research and monitoring.
21. [136s] Solicitation of comments; notice of public hearings.
22. [136t] Delegation and cooperation.
23. [136u] State cooperation, aid, and training.
24. [136v] Authority of States.
25. [136w] Authority of Administrator.
26. [136w–1] State primary enforcement responsibility.
27. [136w–2] Failure by the State to assure enforcement of State pesticide use
regulations.
28. [136w–3] Identification of pests; cooperation with Department of Agriculture’s program.
29. [136w–4] Annual report.
30. [136w–5] Minimum requirements for training of maintenance applicators
and service technicians.
31. [136w–6] Environmental Protection Agency minor use program.
32. [136w–7] Department of Agriculture minor use program.
33. [136w–8] Pesticide registration service fees.
34. [136x] Severability.
35. [136y] Authorization for appropriations.

AN ACT
To regulate the marketing of economic poisons and devices, and for
other purposes.
Be it enacted by the Senate and House of Representatives of the
United States of America in Congress assembled,
1–1 This table of contents is not part of the Act but is included for user convenience. The numbers in brackets refer to section numbers in title 7, United States Code.

1
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SECTION 1. ø7 U.S.C. prec. 121¿ SHORT TITLE AND TABLE OF CONTENTS.

(a) SHORT TITLE.—This Act may be cited as the ‘‘Federal Insecticide, Fungicide, and Rodenticide Act’’.
(b) TABLE OF CONTENTS.— 1–1
Section 1. Short title and table of contents.
(a) Short title.
(b) Table of contents.
Sec. 2. Definitions.
(a) Active ingredient.
(b) Administrator.
(c) Adulterated.
(d) Animal.
(e) Certified applicator, etc.
(1) Certified applicator.
(2) Private applicator.
(3) Commercial applicator.
(4) Under the direct supervision of a certified applicator.
(f) Defoliant.
(g) Desiccant.
(h) Device.
(i) District court.
(j) Environment.
(k) Fungus.
(l) Imminent hazard.
(m) Inert ingredient.
(n) Ingredient statement.
(o) Insect.
(p) Label and labeling.
(1) Label.
(2) Labeling.
(q) Misbranded.
(r) Nematode.
(s) Person.
(t) Pest.
(u) Pesticide.
(v) Plant regulator.
(w) Producer and produce.
(x) Protect health and the environment.
(y) Registrant.
(z) Registration.
(aa) State.
(bb) Unreasonable adverse effects on the environment.
(cc) Weed.
(dd) Establishment.
(ee) To use any registered pesticide in a manner inconsistent with its labeling.
(ff) Outstanding data requirement.
(gg) To distribute or sell.
Sec. 3. Registration of pesticides.
(a) Requirement of registration.
(b) Exemptions.
(c) Procedure for registration.
(1) Statement required.
(2) Data in support of registration.
(3) Time for acting with respect to application.
(4) Notice of application.
(5) Approval of registration.
(6) Denial of registration.
(7) Registration under special circumstances.
(8) Interim administrative review.
(d) Classification of pesticides.
(1) Classification for general use, restricted use, or both.
(2) Change in classification.
1–1 So in original. The table of contents does not correspond to the contents of the Act. Public
Law 104–170 did not make conforming amendments to the table of contents.

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(3) Change in classification from restricted use to general use.
(e) Products with same formulation and claims.
(f) Miscellaneous.
(1) Effect of change of labeling or formulation.
(2) Registration not a defense.
(3) Authority to consult other Federal agencies.
Sec. 4. Reregistration of registered pesticides.
(a) General rule.
(b) Reregistration phases.
(c) Phase one.
(1) Priority for reregistration.
(2) Reregistration lists.
(3) Judicial review.
(4) Notice to registrants.
(d) Phase two.
(1) In general.
(2) Notice of intent to seek or not to seek reregistration.
(3) Missing or inadequate data.
(4) Time periods.
(5) Cancellation and removal.
(6) Suspensions and penalties.
(e) Phase three.
(1) Information about studies.
(2) Time periods.
(3) Cancellation.
(4) Guidelines.
(5) Monitoring.
(f) Phase four.
(1) Independent review and identification of outstanding data requirements.
(2) Time periods.
(3) Suspensions and penalties.
(g) Phase five.
(1) Data review.
(2) Reregistration and other actions.
(h) Compensation of data submitter.
(i) Fees.
(1) Initial fee for food or feed use pesticide active ingredients.
(2) Final fee for food or feed use pesticide active ingredients.
(3) Fees for other pesticide active ingredients.
(4) Reduction or waiver of fees for minor use and other pesticides.
(5) Maintenance fee.
(6) Other fees.
(7) Apportionment.
(j) Exemption of certain registrants.
(k) Reregistration and expedited processing fund.
(1) Establishment.
(2) Source and use.
1–2
Review of inert ingredients; expedited processing of similar applications.
(3)
(4) Unused funds.
(5) Accounting.
(l) Judicial review.
Sec. 5. Experimental use permits.
(a) Issuance.
(b) Temporary tolerance level.
(c) Use under permit.
(d) Studies.
(e) Revocation.
(f) State issuance of permits.
(g) Exemption for agricultural research agencies.
Sec. 6. Administrative review; suspension.
(a) Cancellation after five years.
(1) Procedure.
(2) Information.
(b) Cancellation and change in classification or labels.
1–2 So

in original (as added by sec. 501(g)(1) of P.L. 108–199). Probably should be indented
further.

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(c) Suspension.
(1) Order.
(2) Expedite hearing.
(3) Emergency order.
(4) Judicial review.
(d) Public hearings and scientific review.
(e) Conditional registration.
(f) General provisions.
(1) Voluntary cancellation.
(2) Publication of notice.
(3) Transfer of registration of pesticides registered for minor agricultural
uses.
(g) Notice for stored pesticides with canceled or suspended registrations.
(1) In general.
(2) Copies.
(h) Judicial review.
Sec. 7. Registration of establishments.
(a) Requirements.
(b) Registration.
(c) Information required.
(d) Confidential records and information.
Sec. 8. Records.
(a) Requirement.
(b) Inspection.
Sec. 9. Inspection of establishments, etc.
(a) In general.
(b) Warrants.
(c) Enforcement.
(1) Certification of facts to Attorney General.
(2) Notice not required.
(3) Warning notices.
Sec. 10. Protection of trade secrets and other information.
(a) In general.
(b) Disclosure.
(c) Disputes.
(d) Limitations.
(e) Disclosure to contractors.
(f) Penalty for disclosure by Federal employees.
(g) Disclosure to foreign and multinational pesticide producers.
Sec. 11. Use of restricted use pesticides; applicators.
(a) Certification procedure.
(1) Federal certification.
(2) State certification.
(b) State plans.
(c) Instruction in integrated pest management techniques.
(d) In general.
(e) Separate standards.
Sec. 12. Unlawful acts.
(a) In general.
(b) Exemptions.
Sec. 13. Stop sale, use, removal, and seizure.
(a) Stop sale, etc., orders.
(b) Seizure.
(c) Disposition after condemnation.
(d) Court costs, etc.
Sec. 14. Penalties.
(a) Civil penalties.
(1) In general.
(2) Private applicator.
(3) Hearing.
(4) Determination of penalty.
(5) References to Attorney General.
(b) Criminal penalties.
(1) In general.
(2) Private applicator.
(3) Disclosure of information.
(4) Acts of officers, agents, etc.
Sec. 15. Indemnities.
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(a) General indemnification.
(1) In general.
(2) Exception.
(3) Report.
(4) Appropriation.
(b) Indemnification of end users, dealers, and distributors.
(1) End users.
(2) Dealers and distributors.
(3) Source.
(4) Administrative settlement.
(c) Amount of payment.
(1) In general.
(2) Special rule.
Sec. 16. Administrative procedure; judicial review.
(a) District court review.
(b) Review by Court of Appeals.
(c) Jurisdiction of district courts.
(d) Notice of judgments.
Sec. 17. Imports and exports.
(a) Pesticides and devices intended for export.
(b) Cancellation notices furnished to foreign governments.
(c) Importation of pesticides and devices.
(d) Cooperation in international efforts.
(e) Regulations.
Sec. 18. Exemption of Federal and State agencies.
Sec. 19. Storage, disposal, transportation, and recall.
(a) Storage, disposal, and transportation.
(1) Data requirements and registration of pesticides.
(2) Pesticides.
(3) Containers, rinsates, and other materials.
(b) Recalls.
(1) In general.
(2) Voluntary recall.
(3) Mandatory recall.
(4) Recall procedure.
(5) Contents of recall plan.
(6) Requirements or procedures.
(c) Storage costs.
(1) Submission of plan.
(2) Reimbursement.
(d) Administration of storage, disposal, transportation, and recall programs.
(1) Voluntary agreements.
(2) Rule and regulation review.
(3) Limitations.
(4) Seizure and penalties.
(e) Container design.
(1) Procedures.
(2) Compliance.
(f) Pesticide residue removal.
(1) Procedures.
(2) Compliance.
(3) Solid Waste Disposal Act.
(g) Pesticide container study.
(1) Study.
(2) Report.
(h) Relationship to Solid Waste Disposal Act.
Sec. 20. Research and monitoring.
(a) Research.
(b) National monitoring plan.
(c) Monitoring.
Sec. 21. Solicitation of comments; notice of public hearings.
(a) Secretary of Agriculture.
(b) Views.
(c) Notice.
Sec. 22. Delegation and cooperation.
(a) Delegation.
(b) Cooperation.
Sec. 23. State cooperation, aid, and training.
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(a) Cooperative agreements.
(b) Contracts for training.
(c) Information and education.
Sec. 24. Authority of States.
(a) In general.
(b) Uniformity.
(c) Additional uses.
Sec. 25. Authority of Administrator.
(a) In General.
(1) Regulations.
(2) Procedure.
(3) Congressional committees.
(4) Congressional review of regulations.
(b) Exemption of pesticides.
(c) Other authority.
(d) Scientific advisory panel.
Sec. 26. State primary enforcement responsibility.
(a) In general.
(b) Special rules.
(c) Administrator.
Sec. 27. Failure by the State to assure enforcement of State pesticide use
regulations.
(a) Referral.
(b) Notice.
(c) Construction.
Sec. 28. Identification of pests; cooperation with Department of Agriculture’s
program.
(a) In general.
(b) Pest control availability.
(1) In general.
(2) Report.
(c) Integrated pest management.
Sec. 29. Annual report.
Sec. 30. Minimum requirements for training of maintenance applicators and service
technicians.
Sec. 31. Environmental Protection Agency minor use program.
Sec. 32. Department of Agriculture minor use program.
(a) In general.
(b)(1) Minor use pesticide data.
(2) Minor Use Pesticide Data Revolving Fund.
Sec. 33. Pesticide registration service fees.
(a) Definition of costs.
(b) Fees.
(1) In general.
(2) Covered pesticide registration applications.
(3) Schedule of covered applications and registration service fees.
(4) Pending pesticide registration applications.
(5) Resubmission of pesticide registration applications.
(6) Fee adjustment.
(7) Waivers and reductions.
(8) Refunds.
(c) Pesticide Registration Fund.
(1) Establishment.
(2) Transfers to Fund.
(3) Expenditures from Fund.
(4) Collections and appropriations Acts.
(5) Unused funds.
(d) Assessment of fees.
(1) Definition of covered functions.
(2) Minimum amount of appropriations.
(3) Use of fees.
(4) Compliance.
(5) Subsequent authority.
(e) Reforms to reduce decision time review periods.
(f) Decision time review periods.
(1) In general.
(2) Report.
(3) Applications subject to decision time review periods.
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(4) Start of decision time review period.
(5) Extension of decision time review period.
(g) Judicial review.
(1) In general.
(2) Scope.
(3) Timing.
(4) Remedies.
(h) Accounting.
(i) Auditing.
(1) Financial statements of agencies.
(2) Components.
(3) Inspector General.
(j) Personnel levels.
(k) Reports.
(1) In general.
(2) Contents.
(l) Savings clause.
(m) Termination of effectiveness.
(1) In general.
(2) Phase out.
Sec. 34. Severability.
Sec. 35. Authorization for appropriations.
SEC. 2. ø7 U.S.C. 136¿ DEFINITIONS.

For purposes of this Act—
(a) ACTIVE INGREDIENT.—The term ‘‘active ingredient’’ means—
(1) in the case of a pesticide other than a plant regulator,
defoliant, desiccant, or nitrogen stabilizer, an ingredient which
will prevent, destroy, repel, or mitigate any pest;
(2) in the case of a plant regulator, an ingredient which,
through physiological action, will accelerate or retard the rate
of growth or rate of maturation or otherwise alter the behavior
of ornamental or crop plants or the product thereof;
(3) in the case of a defoliant, an ingredient which will
cause the leaves or foliage to drop from a plant;
(4) in the case of a desiccant, an ingredient which will artificially accelerate the drying of plant tissue; and
(5) in the case of a nitrogen stabilizer, an ingredient which
will prevent or hinder the process of nitrification,
denitrification, ammonia volatilization, or urease production
through action affecting soil bacteria.
(b) ADMINISTRATOR.—The term ‘‘Administrator’’ means the Administrator of the Environmental Protection Agency.
(c) ADULTERATED.—The term ‘‘adulterated’’ applies to any pesticide if—
(1) its strength or purity falls below the professed standard
of quality as expressed on its labeling under which it is sold;
(2) any substance has been substituted wholly or in part
for the pesticide; or
(3) any valuable constituent of the pesticide has been
wholly or in part abstracted.
(d) ANIMAL.—The term ‘‘animal’’ means all vertebrate and invertebrate species, including but not limited to man and other
mammals, birds, fish, and shellfish.
(e) CERTIFIED APPLICATOR, ETC.—
(1) CERTIFIED APPLICATOR.—The term ‘‘certified applicator’’
means any individual who is certified under section 11 as authorized to use or supervise the use of any pesticide which is
classified for restricted use. Any applicator who holds or ap-

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plies registered pesticides, or uses dilutions of registered pesticides consistent with subsection (ee), only to provide a service
of controlling pests without delivering any unapplied pesticide
to any person so served is not deemed to be a seller or distributor of pesticides under this Act.
(2) PRIVATE APPLICATOR.—The term ‘‘private applicator’’
means a certified applicator who uses or supervises the use of
any pesticide which is classified for restricted use for purposes
of producing any agricultural commodity on property owned or
rented by the applicator or the applicator’s employer or (if applied without compensation other than trading of personal
services between producers of agricultural commodities) on the
property of another person.
(3) COMMERCIAL APPLICATOR.—The term ‘‘commercial applicator’’ means an applicator (whether or not the applicator is
a private applicator with respect to some uses) who uses or supervises the use of any pesticide which is classified for restricted use for any purpose or on any property other than as
provided by paragraph (2).
(4) UNDER THE DIRECT SUPERVISION OF A CERTIFIED APPLICATOR.—Unless otherwise prescribed by its labeling, a pesticide shall be considered to be applied under the direct supervision of a certified applicator if it is applied by a competent
person acting under the instructions and control of a certified
applicator who is available if and when needed, even though
such certified applicator is not physically present at the time
and place the pesticide is applied.
(f) DEFOLIANT.—The term ‘‘defoliant’’ means any substance or
mixture of substances intended for causing the leaves or foliage to
drop from a plant, with or without causing abscission.
(g) DESICCANT.—The term ‘‘desiccant’’ means any substance or
mixture of substances intended for artificially accelerating the drying of plant tissue.
(h) DEVICE.—The term ‘‘device’’ means any instrument or contrivance (other than a firearm) which is intended for trapping, destroying, repelling, or mitigating any pest or any other form of
plant or animal life (other than man and other than bacteria, virus,
or other microorganism on or in living man or other living animals); but not including equipment used for the application of pesticides when sold separately therefrom.
(i) DISTRICT COURT.—The term ‘‘district court’’ means a United
States district court, the District Court of Guam, the District Court
of the Virgin Islands, and the highest court of American Samoa.
(j) ENVIRONMENT.—The term ‘‘environment’’ includes water,
air, land, and all plants and man and other animals living therein,
and the interrelationships which exist among these.
(k) FUNGUS.—The term ‘‘fungus’’ means any non-chlorophyllbearing thallophyte (that is, any non-chlorophyll-bearing plant of a
lower order than mosses and liverworts), as for example, rust,
smut, mildew, mold, yeast, and bacteria, except those on or in living man or other animals and those on or in processed food, beverages, or pharmaceuticals.
(l) IMMINENT HAZARD.—The term ‘‘imminent hazard’’ means a
situation which exists when the continued use of a pesticide during
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the time required for cancellation proceeding would be likely to result in unreasonable adverse effects on the environment or will involve unreasonable hazard to the survival of a species declared endangered by the Secretary of the Interior under Public Law 91–
135.
(m) INERT INGREDIENT.—The term ‘‘inert ingredient’’ means an
ingredient which is not active.
(n) INGREDIENT STATEMENT.—The term ‘‘ingredient statement’’
means a statement which contains—
(1) the name and percentage of each active ingredient, and
the total percentage of all inert ingredients, in the pesticide;
and
(2) if the pesticide contains arsenic in any form, a statement of the percentages of total and water soluble arsenic, calculated as elementary arsenic.
(o) INSECT.—The term ‘‘insect’’ means any of the numerous
small invertebrate animals generally having the body more or less
obviously segmented, for the most part belonging to the class
insecta, comprising six-legged, usually winged forms, as for example, beetles, bugs, bees, flies, and to other allied classes of arthropods whose members are wingless and usually have more than six
legs, as for example, spiders, mites, ticks, centipedes, and wood
lice.
(p) LABEL AND LABELING.—
(1) LABEL.—The term ‘‘label’’ means the written, printed,
or graphic matter on, or attached to, the pesticide or device or
any of its containers or wrappers.
(2) LABELING.—The term ‘‘labeling’’ means all labels and
all other written, printed, or graphic matter—
(A) accompanying the pesticide or device at any time;
or
(B) to which reference is made on the label or in literature accompanying the pesticide or device, except to
current official publications of the Environmental Protection Agency, the United States Departments of Agriculture
and Interior, the Department of Health and Human Services, State experiment stations, State agricultural colleges,
and other similar Federal or State institutions or agencies
authorized by law to conduct research in the field of pesticides.
(q) MISBRANDED.—
(1) A pesticide is misbranded if—
(A) its labeling bears any statement, design, or graphic
representation relative thereto or to its ingredients which
is false or misleading in any particular;
(B) it is contained in a package or other container or
wrapping which does not conform to the standards established by the Administrator pursuant to section 25(c)(3);
(C) it is an imitation of, or is offered for sale under the
name of, another pesticide;
(D) its label does not bear the registration number assigned under section 7 to each establishment in which it
was produced;
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(E) any word, statement, or other information required
by or under authority of this Act to appear on the label or
labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements,
designs, or graphic matter in the labeling) and in such
terms as to render it likely to be read and understood by
the ordinary individual under customary conditions of purchase and use;
(F) the labeling accompanying it does not contain directions for use which are necessary for effecting the purpose for which the product is intended and if complied
with, together with any requirements imposed under section 3(d) of this Act, are adequate to protect health and the
environment;
(G) the label does not contain a warning or caution
statement which may be necessary and if complied with,
together with any requirements imposed under section 3(d)
of this Act, is adequate to protect health and the environment; or
(H) in the case of a pesticide not registered in accordance with section 3 of this Act and intended for export, the
label does not contain, in words prominently placed thereon with such conspicuousness (as compared with other
words, statements, designs, or graphic matter in the labeling) as to render it likely to be noted by the ordinary individual under customary conditions of purchase and use,
the following: ‘‘Not Registered for Use in the United States
of America’’.
(2) A pesticide is misbranded if—
(A) the label does not bear an ingredient statement on
that part of the immediate container (and on the outside
container or wrapper of the retail package, if there be one,
through which the ingredient statement on the immediate
container cannot be clearly read) which is presented or displayed under customary conditions of purchase, except
that a pesticide is not misbranded under this subparagraph if—
(i) the size or form of the immediate container, or
the outside container or wrapper of the retail package,
makes it impracticable to place the ingredient statement on the part which is presented or displayed
under customary conditions of purchase; and
(ii) the ingredient statement appears prominently
on another part of the immediate container, or outside
container or wrapper, permitted by the Administrator;
(B) the labeling does not contain a statement of the
use classification under which the product is registered;
(C) there is not affixed to its container, and to the outside container or wrapper of the retail package, if there be
one, through which the required information on the immediate container cannot be clearly read, a label bearing—
(i) the name and address of the producer, registrant, or person for whom produced;
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(ii) the name, brand, or trademark under which
the pesticide is sold;
(iii) the net weight or measure of the content, except that the Administrator may permit reasonable
variations; and
(iv) when required by regulation of the Administrator to effectuate the purposes of this Act, the registration number assigned to the pesticide under this
Act, and the use classification; and
(D) the pesticide contains any substance or substances
in quantities highly toxic to man, unless the label shall
bear, in addition to any other matter required by this
Act—
(i) the skull and crossbones;
(ii) the word ‘‘poison’’ prominently in red on a
background of distinctly contrasting color; and
(iii) a statement of a practical treatment (first aid
or otherwise) in case of poisoning by the pesticide.
(r) NEMATODE.—The term ‘‘nematode’’ means invertebrate animals of the phylum nemathelminthes and class nematoda, that is,
unsegmented round worms with elongated, fusiform, or saclike bodies covered with cuticle, and inhabiting soil, water, plants, or plant
parts; may also be called nemas or eelworms.
(s) PERSON.—The term ‘‘person’’ means any individual, partnership, association, corporation, or any organized group of persons
whether incorporated or not.
(t) PEST.—The term ‘‘pest’’ means (1) any insect, rodent, nematode, fungus, weed, or (2) any other form of terrestrial or aquatic
plant or animal life or virus, bacteria, or other micro-organism (except viruses, bacteria, or other micro-organisms on or in living man
or other living animals) which the Administrator declares to be a
pest under section 25(c)(1).
(u) PESTICIDE.—The term ‘‘pesticide’’ means (1) any substance
or mixture of substances intended for preventing, destroying, repelling, or mitigating any pest, (2) any substance or mixture of substances intended for use as a plant regulator, defoliant, or desiccant, and (3) any nitrogen stabilizer, except that the term ‘‘pesticide’’ shall not include any article that is a ‘‘new animal drug’’
within the meaning of section 201(w) of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C. 321(w)), that has been determined by
the Secretary of Health and Human Services not to be a new animal drug by a regulation establishing conditions of use for the article, or that is an animal feed within the meaning of section 201(x)
of such Act (21 U.S.C. 321(x)) bearing or containing a new animal
drug. The term ‘‘pesticide’’ does not include liquid chemical
sterilant products (including any sterilant or subordinate disinfectant claims on such products) for use on a critical or semi-critical
device, as defined in section 201 of the Federal Food, Drug, and
Cosmetic Act (21 U.S.C. 321). For purposes of the preceding sentence, the term ‘‘critical device’’ includes any device which is introduced directly into the human body, either into or in contact with
the bloodstream or normally sterile areas of the body and the term
‘‘semi-critical device’’ includes any device which contacts intact muSeptember 28, 2012

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cous membranes but which does not ordinarily penetrate the blood
barrier or otherwise enter normally sterile areas of the body.
(v) PLANT REGULATOR.—The term ‘‘plant regulator’’ means any
substance or mixture of substances intended, through physiological
action, for accelerating or retarding the rate of growth or rate of
maturation, or for otherwise altering the behavior of plants or the
produce thereof, but shall not include substances to the extent that
they are intended as plant nutrients, trace elements, nutritional
chemicals, plant inoculants, and soil amendments. Also, the term
‘‘plant regulator’’ shall not be required to include any of such of
those nutrient mixtures or soil amendments as are commonly
known as vitamin-hormone horticultural products, intended for improvement, maintenance, survival, health, and propagation of
plants, and as are not for pest destruction and are nontoxic, nonpoisonous in the undiluted packaged concentration.
(w) PRODUCER AND PRODUCE.—The term ‘‘producer’’ means the
person who manufacturers, prepares, compounds, propagates, or
processes any pesticide or device or active ingredient used in producing a pesticide. The term ‘‘produce’’ means to manufacture, prepare, compound, propagate, or process any pesticide or device or active ingredient used in producing a pesticide. The dilution by individuals of formulated pesticides for their own use and according to
the directions on registered labels shall not of itself result in such
individuals being included in the definition of ‘‘producer’’ for the
purposes of this Act.
(x) PROTECT HEALTH AND THE ENVIRONMENT.—The terms ‘‘protect health and the environment’’ and ‘‘protection of health and the
environment’’ mean protection against any unreasonable adverse
effects on the environment.
(y) REGISTRANT.—The term ‘‘registrant’’ means a person who
has registered any pesticide pursuant to the provisions of this Act.
(z) REGISTRATION.—The term ‘‘registration’’ includes reregistration.
(aa) STATE.—The term ‘‘State’’ means a State, the District of
Columbia, the Commonwealth of Puerto Rico, the Virgin Islands,
Guam, the Trust Territory of the Pacific Islands, and American
Samoa.
(bb) UNREASONABLE ADVERSE EFFECTS ON THE ENVIRONMENT.—The term ‘‘unreasonable adverse effects on the environment’’ means (1) any unreasonable risk to man or the environment,
taking into account the economic, social, and environmental costs
and benefits of the use of any pesticide, or (2) a human dietary risk
from residues that result from a use of a pesticide in or on any food
inconsistent with the standard under section 408 of the Federal
Food, Drug, and Cosmetic Act (21 U.S.C. 346a). 2–1 The Administrator shall consider the risks and benefits of public health pesticides separate from the risks and benefits of other pesticides. In
weighing any regulatory action concerning a public health pesticide
under this Act, the Administrator shall weigh any risks of the pes2–1 Sec. 304 of P.L. 104–170 amended sec. 2(bb) (7 U.S.C. 136(bb)) by inserting ‘‘(1)’’ and ‘‘,
or (2)’’ and all that follows through ‘‘346a).’’, without specifying the Act that was being amended.
The amendments were executed to this Act to effectuate the probable intent of Congress.

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ticide against the health risks such as the diseases transmitted by
the vector to be controlled by the pesticide.
(cc) WEED.—The term ‘‘weed’’ means any plant which grows
where not wanted.
(dd) ESTABLISHMENT.—The term ‘‘establishment’’ means any
place where a pesticide or device or active ingredient used in producing a pesticide is produced, or held, for distribution or sale.
(ee) TO USE ANY REGISTERED PESTICIDE IN A MANNER INCONSISTENT WITH ITS LABELING.—The term ‘‘to use any registered pesticide in a manner inconsistent with its labeling’’ means to use any
registered pesticide in a manner not permitted by the labeling, except that the term shall not include (1) applying a pesticide at any
dosage, concentration, or frequency less than that specified on the
labeling unless the labeling specifically prohibits deviation from the
specified dosage, concentration, or frequency, (2) applying a pesticide against any target pest not specified on the labeling if the
application is to the crop, animal, or site specified on the labeling,
unless the Administrator has required that the labeling specifically
state that the pesticide may be used only for the pests specified on
the labeling after the Administrator has determined that the use
of the pesticide against other pests would cause an unreasonable
adverse effect on the environment, (3) employing any method of application not prohibited by the labeling unless the labeling specifically states that the product may be applied only by the methods
specified on the labeling, (4) mixing a pesticide or pesticides with
a fertilizer when such mixture is not prohibited by the labeling, (5)
any use of a pesticide in conformance with section 5, 18, or 24 of
this Act, or (6) any use of a pesticide in a manner that the Administrator determines to be consistent with the purposes of this Act.
After March 31, 1979, the term shall not include the use of a pesticide for agricultural or forestry purposes at a dilution less than
label dosage unless before or after that date the Administrator
issues a regulation or advisory opinion consistent with the study
provided for in section 27(b) of the Federal Pesticide Act of 1978,
which regulation or advisory opinion specifically requires the use
of definite amounts of dilution.
(ff) OUTSTANDING DATA REQUIREMENT.—
(1) IN GENERAL.—The term ‘‘outstanding data requirement’’ means a requirement for any study, information, or data
that is necessary to make a determination under section 3(c)(5)
and which study, information, or data—
(A) has not been submitted to the Administrator; or
(B) if submitted to the Administrator, the Administrator has determined must be resubmitted because it is
not valid, complete, or adequate to make a determination
under section 3(c)(5) and the regulations and guidelines
issued under such section.
(2) FACTORS.—In making a determination under paragraph
(1)(B) respecting a study, the Administrator shall examine, at
a minimum, relevant protocols, documentation of the conduct
and analysis of the study, and the results of the study to determine whether the study and the results of the study fulfill the
data requirement for which the study was submitted to the
Administrator.
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(gg) TO DISTRIBUTE OR SELL.—The term ‘‘to distribute or sell’’
means to distribute, sell, offer for sale, hold for distribution, hold
for sale, hold for shipment, ship, deliver for shipment, release for
shipment, or receive and (having so received) deliver or offer to deliver. The term does not include the holding or application of registered pesticides or use dilutions thereof by any applicator who
provides a service of controlling pests without delivering any
unapplied pesticide to any person so served.
(hh) NITROGEN STABILIZER.—The term ‘‘nitrogen stabilizer’’
means any substance or mixture of substances intended for preventing or hindering the process of nitrification, denitrification,
ammonia volatilization, or urease production through action upon
soil bacteria. Such term shall not include—
(1) dicyandiamide;
(2) ammonium thiosulfate; or
(3) any substance or mixture of substances.—
(A) that was not registered pursuant to section 3 prior
to January 1, 1992; and
(B) that was in commercial agronomic use prior to
January 1, 1992, with respect to which after January 1,
1992, the distributor or seller of the substance or mixture
has made no specific claim of prevention or hindering of
the process of nitrification, denitrification, ammonia volatilization urease production regardless of the actual use or
purpose for, or future use or purpose for, the substance or
mixture.
Statements made in materials required to be submitted to any
State legislative or regulatory authority, or required by such authority to be included in the labeling or other literature accompanying any such substance or mixture shall not be deemed a specific claim within the meaning of this subsection.
(jj) 2–2 MAINTENANCE APPLICATOR.—The term ‘‘maintenance applicator’’ means any individual who, in the principal course of such
individual’s employment, uses, or supervises the use of, a pesticide
not classified for restricted use (other than a ready to use consumer
products pesticide); for the purpose of providing structural pest
control or lawn pest control including janitors, general maintenance personnel, sanitation personnel, and grounds maintenance
personnel. The term ‘‘maintenance applicator’’ does not include private applicators as defined in section 2(e)(2); individuals who use
antimicrobial pesticides, sanitizers or disinfectants; individuals employed by Federal, State, and local governments or any political
subdivisions thereof, or individuals who use pesticides not classified for restricted use in or around their homes, boats, sod farms,
nurseries, greenhouses, or other noncommercial property.
(kk) SERVICE TECHNICIAN.—The term ‘‘service technician’’
means any individual who uses or supervises the use of pesticides
(other than a ready to use consumer products pesticide) for the
purpose of providing structural pest control or lawn pest control on
the property of another for a fee. The term ‘‘service technician’’
does not include individuals who use antimicrobial pesticides, sani2–2 So in original (as added by sec. 120 of P.L. 104–170). This subsection should probably be
‘‘(ii)’’ and subsequent subsections should be redesignated accordingly.

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tizers or disinfectants; or who otherwise apply ready to use consumer products pesticides.
(ll) MINOR USE.—The term ‘‘minor use’’ means the use of a pesticide on an animal, on a commercial agricultural crop or site, or
for the protection of public health where—
(1) the total United States acreage for the crop is less than
300,000 acres, as determined by the Secretary of Agriculture;
or
(2) the Administrator, in consultation with the Secretary of
Agriculture, determines that, based on information provided by
an applicant for registration or a registrant, the use does not
provide sufficient economic incentive to support the initial registration or continuing registration of a pesticide for such use
and—
(A) there are insufficient efficacious alternative registered pesticides available for the use;
(B) the alternatives to the pesticide use pose greater
risks to the environment or human health;
(C) the minor use pesticide plays or will play a significant part in managing pest resistance; or
(D) the minor use pesticide plays or will play a significant part in an integrated pest management program.
The status as a minor use under this subsection shall continue as
long as the Administrator has not determined that, based on existing data, such use may cause an unreasonable adverse effect on the
environment and the use otherwise qualifies for such status.
(mm) ANTIMICROBIAL PESTICIDE.—
(1) IN GENERAL.—The term ‘‘antimicrobial pesticide’’ means
a pesticide that—
(A) is intended to—
(i) disinfect, sanitize, reduce, or mitigate growth
or development of microbiological organisms; or
(ii) protect inanimate objects, industrial processes
or systems, surfaces, water, or other chemical substances from contamination, fouling, or deterioration
caused by bacteria, viruses, fungi, protozoa, algae, or
slime; and
(B) in the intended use is exempt from, or otherwise
not subject to, a tolerance under section 408 of the Federal
Food, Drug, and Cosmetic Act (21 U.S.C. 346a and 348) or
a food additive regulation under section 409 of such Act.
(2) EXCLUDED PRODUCTS.—The term ‘‘antimicrobial pesticide’’ does not include —
(A) a wood preservative or antifouling paint product
for which a claim of pesticidal activity other than or in addition to an activity described in paragraph (1) is made;
(B) an agricultural fungicide product; or
(C) an aquatic herbicide product.
(3) INCLUDED PRODUCTS.—The term ‘‘antimicrobial pesticide’’ does include any other chemical sterilant product (other
than liquid chemical sterilant products exempt under subsection (u)), any other disinfectant product, any other industrial microbiocide product, and any other preservative product
that is not excluded by paragraph (2).
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(nn) PUBLIC HEALTH PESTICIDE.—The term ‘‘public health pesticide’’ means any minor use pesticide product registered for use
and used predominantly in public health programs for vector control or for other recognized health protection uses, including the
prevention or mitigation of viruses, bacteria, or other microorganisms (other than viruses, bacteria, or other microorganisms on or
in living man or other living animal) that pose a threat to public
health.
(oo) VECTOR.—The term ‘‘vector’’ means any organism capable
of transmitting the causative agent of human disease or capable of
producing human discomfort or injury, including mosquitoes, flies,
fleas, cockroaches, or other insects and ticks, mites, or rats.
SEC. 3. ø7 U.S.C. 136a¿ REGISTRATION OF PESTICIDES.

(a) REQUIREMENT OF REGISTRATION.—Except as provided by
this Act, no person in any State may distribute or sell to any person any pesticide that is not registered under this Act. To the extent necessary to prevent unreasonable adverse effects on the environment, the Administrator may by regulation limit the distribution, sale, or use in any State of any pesticide that is not registered
under this Act and that is not the subject of an experimental use
permit under section 5 or an emergency exemption under section
18.
(b) EXEMPTIONS.—A pesticide which is not registered with the
Administrator may be transferred if—
(1) the transfer is from one registered establishment to another registered establishment operated by the same producer
solely for packaging at the second establishment or for use as
a constituent part of another pesticide produced at the second
establishment; or
(2) the transfer is pursuant to and in accordance with the
requirements of an experimental use permit.
(c) PROCEDURE FOR REGISTRATION.—
(1) STATEMENT REQUIRED.—Each applicant for registration
of a pesticide shall file with the Administrator a statement
which includes—
(A) the name and address of the applicant and of any
other person whose name will appear on the labeling;
(B) the name of the pesticide;
(C) a complete copy of the labeling of the pesticide, a
statement of all claims to be made for it, and any directions for its use;
(D) the complete formula of the pesticide;
(E) a request that the pesticide be classified for general use or for restricted use, or for both; and
(F) except as otherwise provided in paragraph (2)(D),
if requested by the Administrator, a full description of the
tests made and the results thereof upon which the claims
are based, or alternatively a citation to data that appear
in the public literature or that previously had been submitted to the Administrator and that the Administrator
may consider in accordance with the following provisions:
(i) With respect to pesticides containing active ingredients that are initially registered under this Act
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after the date of enactment of the Federal Pesticide
Act of 1978 [September 30, 1978], data submitted to
support the application for the original registration of
the pesticide, or an application for an amendment adding any new use to the registration and that pertains
solely to such new use, shall not, without the written
permission of the original data submitter, be considered by the Administrator to support an application by
another person during a period of ten years following
the date the Administrator first registers the pesticide,
except that such permission shall not be required in
the case of defensive data.
(ii) The period of exclusive data use provided
under clause (i) shall be extended 1 additional year for
each 3 minor uses registered after the date of enactment of this clause [Aug. 3, 1996] and within 7 years
of the commencement of the exclusive use period, up
to a total of 3 additional years for all minor uses registered by the Administrator if the Administrator, in
consultation with the Secretary of Agriculture, determines that, based on information provided by an applicant for registration or a registrant, that—
(I) there are insufficient efficacious alternative registered pesticides available for the use;
(II) the alternatives to the minor use pesticide
pose greater risks to the environment or human
health;
(III) the minor use pesticide plays or will play
a significant part in managing pest resistance; or
(IV) the minor use pesticide plays or will play
a significant part in an integrated pest management program.
The registration of a pesticide for a minor use on a
crop grouping established by the Administrator shall
be considered for purposes of this clause 1 minor use
for each representative crop for which data are provided in the crop grouping. Any additional exclusive
use period under this clause shall be modified as appropriate or terminated if the registrant voluntarily
cancels the product or deletes from the registration
the minor uses which formed the basis for the extension of the additional exclusive use period or if the Administrator determines that the registrant is not actually marketing the product for such minor uses.
(iii) Except as otherwise provided in clause (i),
with respect to data submitted after December 31,
1969, by an applicant or registrant to support an application for registration, experimental use permit, or
amendment adding a new use to an existing registration, to support or maintain in effect an existing registration, or for reregistration, the Administrator may,
without the permission of the original data submitter,
consider any such item of data in support of an application by any other person (hereinafter in this subSeptember 28, 2012

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paragraph referred to as the ‘‘applicant’’) within the
fifteen-year period following the date the data were
originally submitted only if the applicant has made an
offer to compensate the original data submitter and
submitted such offer to the Administrator accompanied by evidence of delivery to the original data submitter of the offer. The terms and amount of compensation may be fixed by agreement between the
original data submitter and the applicant, or, failing
such agreement, binding arbitration under this subparagraph. If, at the end of ninety days after the date
of delivery to the original data submitter of the offer
to compensate, the original data submitter and the applicant have neither agreed on the amount and terms
of compensation nor on a procedure for reaching an
agreement on the amount and terms of compensation,
either person may initiate binding arbitration proceedings by requesting the Federal Mediation and
Conciliation Service to appoint an arbitrator from the
roster of arbitrators maintained by such Service. The
procedure and rules of the Service shall be applicable
to the selection of such arbitrator and to such arbitration proceedings, and the findings and determination
of the arbitrator shall be final and conclusive, and no
official or court of the United States shall have power
or jurisdiction to review any such findings and determination, except for fraud, misrepresentation, or other
misconduct by one of the parties to the arbitration or
the arbitrator where there is a verified complaint with
supporting affidavits attesting to specific instances of
such fraud, misrepresentation, or other misconduct.
The parties to the arbitration shall share equally in
the payment of the fee and expenses of the arbitrator.
If the Administrator determines that an original data
submitter has failed to participate in a procedure for
reaching an agreement or in an arbitration proceeding
as required by this subparagraph, or failed to comply
with the terms of an agreement or arbitration decision
concerning compensation under this subparagraph, the
original data submitter shall forfeit the right to compensation for the use of the data in support of the application. Notwithstanding any other provision of this
Act, if the Administrator determines that an applicant
has failed to participate in a procedure for reaching an
agreement or in an arbitration proceeding as required
by this subparagraph, or failed to comply with the
terms of an agreement or arbitration decision concerning compensation under this subparagraph, the
Administrator shall deny the application or cancel the
registration of the pesticide in support of which the
data were used without further hearing. Before the
Administrator takes action under either of the preceding two sentences, the Administrator shall furnish
to the affected person, by certified mail, notice of inSeptember 28, 2012

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tent to take action and allow fifteen days from the
date of delivery of the notice for the affected person to
respond. If a registration is denied or canceled under
this subparagraph, the Administrator may make such
order as the Administrator deems appropriate concerning the continued sale and use of existing stocks
of such pesticide. Registration action by the Administrator shall not be delayed pending the fixing of compensation.
(iv) After expiration of any period of exclusive use
and any period for which compensation is required for
the use of an item of data under clauses (i), (ii), and
(iii), the Administrator may consider such item of data
in support of an application by any other applicant
without the permission of the original data submitter
and without an offer having been received to compensate the original data submitter for the use of such
item of data.
(v) The period of exclusive use provided under
clause (ii) shall not take effect until 1 year after enactment of this clause [Aug. 3, 1996], except where an applicant or registrant is applying for the registration of
a pesticide containing an active ingredient not previously registered.
(vi) With respect to data submitted after the date
of enactment of this clause [Aug. 3, 1996] by an applicant or registrant to support an amendment adding a
new use to an existing registration that does not retain any period of exclusive use, if such data relates
solely to a minor use of a pesticide, such data shall
not, without the written permission of the original
data submitter, be considered by the Administrator to
support an application for a minor use by another person during the period of 10 years following the date of
submission of such data. The applicant or registrant at
the time the new minor use is requested shall notify
the Administrator that to the best of their knowledge
the exclusive use period for the pesticide has expired
and that the data pertaining solely to the minor use
of a pesticide is eligible for the provisions of this paragraph. If the minor use registration which is supported by data submitted pursuant to this subsection
is voluntarily canceled or if such data are subsequently used to support a nonminor use, the data shall
no longer be subject to the exclusive use provisions of
this clause but shall instead be considered by the Administrator in accordance with the provisions of clause
(i), as appropriate.
(G) If the applicant is requesting that the registration
or amendment to the registration of a pesticide be expedited, an explanation of the basis for the request must be
submitted, in accordance with paragraph (10) of this subsection.
(2) DATA IN SUPPORT OF REGISTRATION.—
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(A) IN GENERAL.—The Administrator shall publish
guidelines specifying the kinds of information which will
be required to support the registration of a pesticide and
shall revise such guidelines from time to time. If thereafter
the Administrator requires any additional kind of information under subparagraph (B) of this paragraph, the Administrator shall permit sufficient time for applicants to obtain such additional information. The Administrator, in establishing standards for data requirements for the registration of pesticides with respect to minor uses, shall
make such standards commensurate with the anticipated
extent of use, pattern of use, the public health and agricultural need for such minor use, and the level and degree of
potential beneficial or adverse effects on man and the environment. The Administrator shall not require a person to
submit, in relation to a registration or reregistration of a
pesticide for minor agricultural use under this Act, any
field residue data from a geographic area where the pesticide will not be registered for such use. In the development of these standards, the Administrator shall consider
the economic factors of potential national volume of use,
extent of distribution, and the impact of the cost of meeting the requirements on the incentives for any potential
registrant to undertake the development of the required
data. Except as provided by section 10, within 30 days
after the Administrator registers a pesticide under this Act
the Administrator shall make available to the public the
data called for in the registration statement together with
such other scientific information as the Administrator
deems relevant to the Administrator’s decision.
(B) ADDITIONAL DATA.—(i) If the Administrator determines that additional data are required to maintain in effect an existing registration of a pesticide, the Administrator shall notify all existing registrants of the pesticide
to which the determination relates and provide a list of
such registrants to any interested person.
(ii) Each registrant of such pesticide shall provide evidence within ninety days after receipt of notification that
it is taking appropriate steps to secure the additional data
that are required. Two or more registrants may agree to
develop jointly, or to share in the cost of developing, such
data if they agree and advise the Administrator of their intent within ninety days after notification. Any registrant
who agrees to share in the cost of producing the data shall
be entitled to examine and rely upon such data in support
of maintenance of such registration. The Administrator
shall issue a notice of intent to suspend the registration of
a pesticide in accordance with the procedures prescribed
by clause (iv) if a registrant fails to comply with this
clause.
(iii) If, at the end of sixty days after advising the Administrator of their agreement to develop jointly, or share
in the cost of developing data, the registrants have not further agreed on the terms of the data development arrangeSeptember 28, 2012

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ment or on a procedure for reaching such agreement, any
of such registrants may initiate binding arbitration proceedings by requesting the Federal Mediation and Conciliation Service to appoint an arbitrator from the roster of
arbitrators maintained by such Service. The procedure and
rules of the Service shall be applicable to the selection of
such arbitrator and to such arbitration proceedings, and
the findings and determination of the arbitrator shall be
final and conclusive, and no official or court of the United
States shall have power or jurisdiction to review any such
findings and determination, except for fraud, misrepresentation, or other misconduct by one of the parties to the arbitration or the arbitrator where there is a verified complaint with supporting affidavits attesting to specific instances of such fraud, misrepresentation, or other misconduct. All parties to the arbitration shall share equally
in the payment of the fee and expenses of the arbitrator.
The Administrator shall issue a notice of intent to suspend
the registration of a pesticide in accordance with the procedures prescribed by clause (iv) if a registrant fails to comply with this clause.
(iv) Notwithstanding any other provision of this Act, if
the Administrator determines that a registrant, within the
time required by the Administrator, has failed to take appropriate steps to secure the data required under this subparagraph, to participate in a procedure for reaching
agreement concerning a joint data development arrangement under this subparagraph or in an arbitration proceeding as required by this subparagraph, or to comply
with the terms of an agreement or arbitration decision concerning a joint data development arrangement under this
subparagraph, the Administrator may issue a notice of intent to suspend such registrant’s registration of the pesticide for which additional data is required. The Administrator may include in the notice of intent to suspend such
provisions as the Administrator deems appropriate concerning the continued sale and use of existing stocks of
such pesticide. Any suspension proposed under this subparagraph shall become final and effective at the end of
thirty days from receipt by the registrant of the notice of
intent to suspend, unless during that time a request for
hearing is made by a person adversely affected by the notice or the registrant has satisfied the Administrator that
the registrant has complied fully with the requirements
that served as a basis for the notice of intent to suspend.
If a hearing is requested, a hearing shall be conducted
under section 6(d) of this Act. The only matters for resolution at that hearing shall be whether the registrant has
failed to take the action that served as the basis for the
notice of intent to suspend the registration of the pesticide
for which additional data is required, and whether the Administrator’s determination with respect to the disposition
of existing stocks is consistent with this Act. If a hearing
is held, a decision after completion of such hearing shall
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be final. Notwithstanding any other provision of this Act,
a hearing shall be held and a determination made within
seventy-five days after receipt of a request for such hearing. Any registration suspended under this subparagraph
shall be reinstated by the Administrator if the Administrator determines that the registrant has complied fully
with the requirements that served as a basis for the suspension of the registration.
(v) Any data submitted under this subparagraph shall
be subject to the provisions of paragraph (1)(D). Whenever
such data are submitted jointly by two or more registrants,
an agent shall be agreed on at the time of the joint submission to handle any subsequent data compensation matters for the joint submitters of such data.
(vi) Upon the request of a registrant the Administrator
shall, in the case of a minor use, extend the deadline for
the production of residue chemistry data under this subparagraph for data required solely to support that minor
use until the final deadline for submission of data under
section 4 for the other uses of the pesticide established as
of the date of enactment of the Food Quality Protection Act
of 1996 [Aug. 3, 1996], if—
(I) the data to support other uses of the pesticide
on a food are being provided;
(II) the registrant, in submitting a request for
such an extension, provides a schedule, including interim dates to measure progress, to assure that the
data production will be completed before the expiration of the extension period;
(III) the Administrator has determined that such
extension will not significantly delay the Administrator’s schedule for issuing a reregistration eligibility determination required under section 4; and
(IV) the Administrator has determined that based
on existing data, such extension would not significantly increase the risk of any unreasonable adverse
effect on the environment. 3–1 If the Administrator
grants an extension under this clause, the Administrator shall monitor the development of the data and
shall ensure that the registrant is meeting the schedule for the production of the data. If the Administrator
determines that the registrant is not meeting or has
not met the schedule for the production of such data,
the Administrator may proceed in accordance with
clause (iv) regarding the continued registration of the
affected products with the minor use and shall inform
the public of such action. Notwithstanding the provisions of this clause, the Administrator may take action
to modify or revoke the extension under this clause if
the Administrator determines that the extension for
the minor use may cause an unreasonable adverse ef3–1 Indentation of the following sentences of this clause is so in original (as added by sec.
201(c)(1) of P.L. 104–170). Probably should be indented the same as flush matter of this clause.

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fect on the environment. In such circumstance, the Administrator shall provide, in writing to the registrant,
a notice revoking the extension of time for submission
of data. Such data shall instead be due in accordance
with the date established by the Administrator for the
submission of the data.
(vii) If the registrant does not commit to support a
specific minor use of the pesticide, but is supporting and
providing data in a timely and adequate fashion to support
uses of the pesticide on a food, or if all uses of the pesticide are nonfood uses and the registrant does not commit
to support a specific minor use of the pesticide but is supporting and providing data in a timely and adequate fashion to support other nonfood uses of the pesticide, the Administrator, at the written request of the registrant, shall
not take any action pursuant to this clause in regard to
such unsupported minor use until the final deadline established as of the date of enactment of the Food Quality Protection Act of 1996 [Aug. 3, 1996], for the submission of
data under section 4 for the supported uses identified pursuant to this clause unless the Administrator determines
that the absence of the data is significant enough to cause
human health or environmental concerns. On the basis of
such determination, the Administrator may refuse the request for extension by the registrant. Upon receipt of the
request from the registrant, the Administrator shall publish in the Federal Register a notice of the receipt of the
request and the effective date upon which the uses not
being supported will be voluntarily deleted from the registration pursuant to section 6(f)(1). If the Administrator
grants an extension under this clause, the Administrator
shall monitor the development of the data for the uses
being supported and shall ensure that the registrant is
meeting the schedule for the production of such data. If
the Administrator determines that the registrant is not
meeting or has not met the schedule for the production of
such data, the Administrator may proceed in accordance
with clause (iv) of this subparagraph regarding the continued registration of the affected products with the minor
and other uses and shall inform the public of such action
in accordance with section 6(f)(2). Notwithstanding the
provisions of this clause, the Administrator may deny,
modify, or revoke the temporary extension under this subparagraph if the Administrator determines that the continuation of the minor use may cause an unreasonable adverse effect on the environment. In the event of modification or revocation, the Administrator shall provide, in writing, to the registrant a notice revoking the temporary extension and establish a new effective date by which the
minor use shall be deleted from the registration.
(viii)(I) If data required to support registration of a
pesticide under subparagraph (A) is requested by a Federal or State regulatory authority, the Administrator shall,
to the extent practicable, coordinate data requirements,
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test protocols, timetables, and standards of review and reduce burdens and redundancy caused to the registrant by
multiple requirements on the registrant.
(II) The Administrator may enter into a cooperative
agreement with a State to carry out subclause (I).
(III) Not later than 1 year after the date of enactment
of this clause [Aug. 3, 1996], the Administrator shall develop a process to identify and assist in alleviating future
disparities between Federal and State data requirements.
(C) SIMPLIFIED PROCEDURES.—Within nine months
after the date of enactment of this subparagraph [September 30, 1978], the Administrator shall, by regulation,
prescribe simplified procedures for the registration of pesticides, which shall include the provisions of subparagraph
(D) of this paragraph.
(D) EXEMPTION.—No applicant for registration of a
pesticide who proposes to purchase a registered pesticide
from another producer in order to formulate such purchased pesticide into the pesticide that is the subject of the
application shall be required to—
(i) submit or cite data pertaining to such purchased product; or
(ii) offer to pay reasonable compensation otherwise
required by paragraph (1)(D) of this subsection for the
use of any such data.
(E) MINOR USE WAIVER.—In handling the registration
of a pesticide for a minor use, the Administrator may
waive otherwise applicable data requirements if the Administrator determines that the absence of such data will
not prevent the Administrator from determining—
(i) the incremental risk presented by the minor
use of the pesticide; and
(ii) that such risk, if any, would not be an unreasonable adverse effect on the environment.
(3) TIME FOR ACTING WITH RESPECT TO APPLICATION.—
(A) IN GENERAL.—The Administrator shall review the
data after receipt of the application and shall, as expeditiously as possible, either register the pesticide in accordance with paragraph (5), or notify the applicant of the Administrator’s determination that it does not comply with
the provisions of the Act in accordance with paragraph (6).
(B) IDENTICAL OR SUBSTANTIALLY SIMILAR.—(i) The Administrator shall, as expeditiously as possible, review and
act on any application received by the Administrator
that—
(I) proposes the initial or amended registration of
an end-use pesticide that, if registered as proposed,
would be identical or substantially similar in composition and labeling to a currently-registered pesticide
identified in the application, or that would differ in
composition and labeling from such currently-registered pesticide only in ways that would not significantly increase the risk of unreasonable adverse effects on the environment; or
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(II) proposes an amendment to the registration of
a registered pesticide that does not require scientific
review of data.
(ii) In expediting the review of an application for an
action described in clause (i), the Administrator shall—
(I) review the application in accordance with section 33(f)(4)(B) and, if the application is found to be incomplete, reject the application;
(II) not later than the applicable decision review
time established pursuant to section 33(f)(4)(B), or, if
no review time is established, not later than 90 days
after receiving a complete application, notify the registrant if the application has been granted or denied;
and
(III) if the application is denied, notify the registrant in writing of the specific reasons for the denial
of the application.
(C) MINOR USE REGISTRATION.—
(i) The Administrator shall, as expeditiously as
possible, review and act on any complete application—
(I) that proposes the initial registration of a
new pesticide active ingredient if the active ingredient is proposed to be registered solely for minor
uses, or proposes a registration amendment solely
for minor uses to an existing registration; or
(II) for a registration or a registration amendment that proposes significant minor uses.
(ii) For the purposes of clause (i)—
(I) the term ‘‘as expeditiously as possible’’
means that the Administrator shall, to the greatest extent practicable, complete a review and evaluation of all data, submitted with a complete application, within 12 months after the submission
of the complete application, and the failure of the
Administrator to complete such a review and evaluation under clause (i) shall not be subject to judicial review; and
(II) the term ‘‘significant minor uses’’ means 3
or more minor uses proposed for every nonminor
use, a minor use that would, in the judgment of
the Administrator, serve as a replacement for any
use which has been canceled in the 5 years preceding the receipt of the application, or a minor
use that in the opinion of the Administrator would
avoid the reissuance of an emergency exemption
under section 18 for that minor use.
(D) ADEQUATE TIME FOR SUBMISSION OF MINOR USE
DATA.—If a registrant makes a request for a minor use
waiver, regarding data required by the Administrator, pursuant to paragraph (2)(E), and if the Administrator denies
in whole or in part such data waiver request, the registrant shall have a full-time period for providing such
data. For purposes of this subparagraph, the term ‘‘fulltime period’’ means the time period originally established
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by the Administrator for submission of such data, beginning with the date of receipt by the registrant of the Administrator’s notice of denial.
(4) NOTICE OF APPLICATION.—The Administrator shall publish in the Federal Register, promptly after receipt of the statement and other data required pursuant to paragraphs (1) and
(2), a notice of each application for registration of any pesticide
if it contains any new active ingredient or if it would entail a
changed use pattern. The notice shall provide for a period of
30 days in which any Federal agency or any other interested
person may comment.
(5) APPROVAL OF REGISTRATION.—The Administrator shall
register a pesticide if the Administrator determines that, when
considered with any restrictions imposed under subsection
(d)—
(A) its composition is such as to warrant the proposed
claims for it;
(B) its labeling and other material required to be submitted comply with the requirements of this Act;
(C) it will perform its intended function without unreasonable adverse effects on the environment; and
(D) when used in accordance with widespread and
commonly recognized practice it will not generally cause
unreasonable adverse effects on the environment.
The Administrator shall not make any lack of essentiality a
criterion for denying registration of any pesticide. Where two
pesticides meet the requirements of this paragraph, one should
not be registered in preference to the other. In considering an
application for the registration of a pesticide, the Administrator may waive data requirements pertaining to efficacy, in
which event the Administrator may register the pesticide without determining that the pesticide’s composition is such as to
warrant proposed claims of efficacy. If a pesticide is found to
be efficacious by any State under section 24(c) of this Act, a
presumption is established that the Administrator shall waive
data requirements pertaining to efficacy for use of the pesticide
in such State.
(6) DENIAL OF REGISTRATION.—If the Administrator determines that the requirements of paragraph (5) for registration
are not satisfied, the Administrator shall notify the applicant
for registration of the Administrator’s determination and of the
Administrator’s reasons (including the factual basis) therefor,
and that, unless the applicant corrects the conditions and notifies the Administrator thereof during the 30-day period beginning with the day after the date on which the applicant receives the notice, the Administrator may refuse to register the
pesticide. Whenever the Administrator refuses to register a
pesticide, the Administrator shall notify the applicant of the
Administrator’s decision and of the Administrator’s reasons (including the factual basis) therefor. The Administrator shall
promptly publish in the Federal Register notice of such denial
of registration and the reasons therefor. Upon such notification, the applicant for registration or other interested person
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with the concurrence of the applicant shall have the same remedies as provided for in section 6.
(7) REGISTRATION UNDER SPECIAL CIRCUMSTANCES.—Notwithstanding the provisions of paragraph (5)—
(A) The Administrator may conditionally register or
amend the registration of a pesticide if the Administrator
determines that (i) the pesticide and proposed use are
identical or substantially similar to any currently registered pesticide and use thereof, or differ only in ways
that would not significantly increase the risk of unreasonable adverse effects on the environment, and (ii) approving
the registration or amendment in the manner proposed by
the applicant would not significantly increase the risk of
any unreasonable adverse effect on the environment. An
applicant seeking conditional registration or amended registration under this subparagraph shall submit such data
as would be required to obtain registration of a similar
pesticide under paragraph (5). If the applicant is unable to
submit an item of data because it has not yet been generated, the Administrator may register or amend the registration of the pesticide under such conditions as will require the submission of such data not later than the time
such data are required to be submitted with respect to
similar pesticides already registered under this Act.
(B) The Administrator may conditionally amend the
registration of a pesticide to permit additional uses of such
pesticide notwithstanding that data concerning the pesticide may be insufficient to support an unconditional
amendment, if the Administrator determines that (i) the
applicant has submitted satisfactory data pertaining to the
proposed additional use, and (ii) amending the registration
in the manner proposed by the applicant would not significantly increase the risk of any unreasonable adverse effect
on the environment. Notwithstanding the foregoing provisions of this subparagraph, no registration of a pesticide
may be amended to permit an additional use of such pesticide if the Administrator has issued a notice stating that
such pesticide, or any ingredient thereof, meets or exceeds
risk criteria associated in whole or in part with human dietary exposure enumerated in regulations issued under
this Act, and during the pendency of any risk-benefit evaluation initiated by such notice, if (I) the additional use of
such pesticide involves a major food or feed crop, or (II) the
additional use of such pesticide involves a minor food or
feed crop and the Administrator determines, with the concurrence of the Secretary of Agriculture, there is available
an effective alternative pesticide that does not meet or exceed such risk criteria. An applicant seeking amended registration under this subparagraph shall submit such data
as would be required to obtain registration of a similar
pesticide under paragraph (5). If the applicant is unable to
submit an item of data (other than data pertaining to the
proposed additional use) because it has not yet been generated, the Administrator may amend the registration
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under such conditions as will require the submission of
such data not later than the time such data are required
to be submitted with respect to similar pesticides already
registered under this Act.
(C) The Administrator may conditionally register a
pesticide containing an active ingredient not contained in
any currently registered pesticide for a period reasonably
sufficient for the generation and submission of required
data (which are lacking because a period reasonably sufficient for generation of the data has not elapsed since the
Administrator first imposed the data requirement) on the
condition that by the end of such period the Administrator
receives such data and the data do not meet or exceed risk
criteria enumerated in regulations issued under this Act,
and on such other conditions as the Administrator may
prescribe. A conditional registration under this subparagraph shall be granted only if the Administrator determines that use of the pesticide during such period will not
cause any unreasonable adverse effect on the environment,
and that use of the pesticide is in the public interest.
(8) INTERIM ADMINISTRATIVE REVIEW.—Notwithstanding
any other provision of this Act, the Administrator may not initiate a public interim administrative review process to develop
a risk-benefit evaluation of the ingredients of a pesticide or any
of its uses prior to initiating a formal action to cancel, suspend,
or deny registration of such pesticide, required under this Act,
unless such interim administrative process is based on a validated test or other significant evidence raising prudent concerns of unreasonable adverse risk to man or to the environment. Notice of the definition of the terms ‘‘validated test’’ and
‘‘other significant evidence’’ as used herein shall be published
by the Administrator in the Federal Register.
(9) LABELING.—
(A) ADDITIONAL STATEMENTS.—Subject to subparagraphs (B) and (C), it shall not be a violation of this Act
for a registrant to modify the labeling of an antimicrobial
pesticide product to include relevant information on product efficacy, product composition, container composition or
design, or other characteristics that do not relate to any
pesticidal claim or pesticidal activity.
(B) REQUIREMENTS.—Proposed labeling information
under subparagraph (A) shall not be false or misleading,
shall not conflict with or detract from any statement required by law or the Administrator as a condition of registration, and shall be substantiated on the request of the
Administrator.
(C) NOTIFICATION AND DISAPPROVAL.—
(i) NOTIFICATION.—A registration may be modified
under subparagraph (A) if —
(I) the registrant notifies the Administrator in
writing not later than 60 days prior to distribution
or sale of a product bearing the modified labeling;
and
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(II) the Administrator does not disapprove of
the modification under clause (ii).
(ii) DISAPPROVAL.—Not later than 30 days after
receipt of a notification under clause (i), the Administrator may disapprove the modification by sending the
registrant notification in writing stating that the proposed language is not acceptable and stating the reasons why the Administrator finds the proposed modification unacceptable.
(iii) RESTRICTION ON SALE.—A registrant may not
sell or distribute a product bearing a disapproved
modification.
(iv) OBJECTION.—A registrant may file an objection in writing to a disapproval under clause (ii) not
later than 30 days after receipt of notification of the
disapproval.
(v) FINAL ACTION.—A decision by the Administrator following receipt and consideration of an objection filed under clause (iv) shall be considered a final
agency action.
(D) USE DILUTION.—The label or labeling required
under this Act for an antimicrobial pesticide that is or may
be diluted for use may have a different statement of caution or protective measures for use of the recommended diluted solution of the pesticide than for use of a concentrate
of the pesticide if the Administrator determines that —
(i) adequate data have been submitted to support
the statement proposed for the diluted solution uses;
and
(ii) the label or labeling provides adequate protection for exposure to the diluted solution of the pesticide.
(10) EXPEDITED REGISTRATION OF PESTICIDES.—
(A) Not later than 1 year after the date of enactment
of this paragraph [Aug. 3, 1996], the Administrator shall,
utilizing public comment, develop procedures and guidelines, and expedite the review of an application for registration of a pesticide or an amendment to a registration
that satisfies such guidelines.
(B) Any application for registration or an amendment,
including biological and conventional pesticides, will be
considered for expedited review under this paragraph. An
application for registration or an amendment shall qualify
for expedited review if use of the pesticide proposed by the
application may reasonably be expected to accomplish 1 or
more of the following:
(i) Reduce the risks of pesticides to human health.
(ii) Reduce the risks of pesticides to nontarget organisms.
(iii) Reduce the potential for contamination of
groundwater, surface water, or other valued environmental resources.
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(iv) Broaden the adoption of integrated pest management strategies, or make such strategies more
available or more effective.
(C) The Administrator, not later than 30 days after receipt of an application for expedited review, shall notify
the applicant whether the application is complete. If it is
found to be incomplete, the Administrator may either reject the request for expedited review or ask the applicant
for additional information to satisfy the guidelines developed under subparagraph (A).
(d) CLASSIFICATION OF PESTICIDES.—
(1) CLASSIFICATION FOR GENERAL USE, RESTRICTED USE, OR
BOTH.—
(A) As a part of the registration of a pesticide the Administrator shall classify it as being for general use or for
restricted use. If the Administrator determines that some
of the uses for which the pesticide is registered should be
for general use and that other uses for which it is registered should be for restricted use, the Administrator
shall classify it for both general use and restricted use.
Pesticide uses may be classified by regulation on the initial
classification and registered pesticides may be classified
prior to reregistration. If some of the uses of the pesticide
are classified for general use and other uses are classified
for restricted use, the directions relating to its general
uses shall be clearly separated and distinguished from
those directions relating to its restricted uses. The Administrator may require that its packaging and labeling for restricted uses shall be clearly distinguishable from its packaging and labeling for general uses.
(B) If the Administrator determines that the pesticide,
when applied in accordance with its directions for use,
warnings and cautions and for the uses for which it is registered, or for one or more of such uses, or in accordance
with a widespread and commonly recognized practice, will
not generally cause unreasonable adverse effects on the
environment, the Administrator will classify the pesticide,
or the particular use or uses of the pesticide to which the
determination applies, for general use.
(C) If the Administrator determines that the pesticide,
when applied in accordance with its directions for use,
warnings and cautions and for the uses for which it is registered, or for one or more of such uses, or in accordance
with a widespread and commonly recognized practice, may
generally cause, without additional regulatory restrictions,
unreasonable adverse effects on the environment, including injury to the applicator, the Administrator shall classify the pesticide, or the particular use or uses to which
the determination applies, for restricted use:
(i) If the Administrator classifies a pesticide, or
one or more uses of such pesticide, for restricted use
because of a determination that the acute dermal or
inhalation toxicity of the pesticide presents a hazard
to the applicator or other persons, the pesticide shall
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be applied for any use to which the restricted classification applies only by or under the direct supervision
of a certified applicator.
(ii) If the Administrator classifies a pesticide, or
one or more uses of such pesticide, for restricted use
because of a determination that its use without additional regulatory restriction may cause unreasonable
adverse effects on the environment, the pesticide shall
be applied for any use to which the determination applies only by or under the direct supervision of a certified applicator, or subject to such other restrictions
as the Administrator may provide by regulation. Any
such regulation shall be reviewable in the appropriate
court of appeals upon petition of a person adversely affected filed within 60 days of the publication of the
regulation in final form.
(2) CHANGE IN CLASSIFICATION.—If the Administrator determines that a change in the classification of any use of a pesticide from general use to restricted use is necessary to prevent
unreasonable adverse effects on the environment, the Administrator shall notify the registrant of such pesticide of such determination at least forty-five days before making the change
and shall publish the proposed change in the Federal Register.
The registrant, or other interested person with the concurrence
of the registrant, may seek relief from such determination
under section 6(b).
(3) CHANGE IN CLASSIFICATION FROM RESTRICTED USE TO
GENERAL USE.—The registrant of any pesticide with one or
more uses classified for restricted use may petition the Administrator to change any such classification from restricted to
general use. Such petition shall set out the basis for the registrant’s position that restricted use classification is unnecessary because classification of the pesticide for general use
would not cause unreasonable adverse effects on the environment. The Administrator, within sixty days after receiving
such petition, shall notify the registrant whether the petition
has been granted or denied. Any denial shall contain an explanation therefor and any such denial shall be subject to judicial
review under section 16 of this Act.
(e) PRODUCTS WITH SAME FORMULATION AND CLAIMS.—Products which have the same formulation, are manufactured by the
same person, the labeling of which contains the same claims, and
the labels of which bear a designation identifying the product as
the same pesticide may be registered as a single pesticide; and additional names and labels shall be added to the registration by supplemental statements.
(f) MISCELLANEOUS.—
(1) EFFECT OF CHANGE OF LABELING OR FORMULATION.—If
the labeling or formulation for a pesticide is changed, the registration shall be amended to reflect such change if the Administrator determines that the change will not violate any provision of this Act.
(2) REGISTRATION NOT A DEFENSE.—In no event shall registration of an article be construed as a defense for the comSeptember 28, 2012

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mission of any offense under this Act. As long as no cancellation proceedings are in effect registration of a pesticide shall
be prima facie evidence that the pesticide, its labeling and
packaging comply with the registration provisions of the Act.
(3) AUTHORITY TO CONSULT OTHER FEDERAL AGENCIES.—In
connection with consideration of any registration or application
for registration under this section, the Administrator may consult with any other Federal agency.
(4) MIXTURES OF NITROGEN STABILIZERS AND FERTILIZER
PRODUCTS.—Any mixture or other combination of—
(A) 1 or more nitrogen stabilizers registered under this
Act; and
(B) 1 or more fertilizer products,
shall not be subject to the provisions of this section or sections
4, 5, 7, 15, and 17(a)(2) if the mixture or other combination is
accompanied by the labeling required under this Act for the nitrogen stabilizer contained in the mixture or other combination, the mixture or combination is mixed or combined in accordance with such labeling, and the mixture or combination
does not contain any active ingredient other than the nitrogen
stabilizer.
(g) REGISTRATION REVIEW.—
(1)(A) GENERAL RULE.—
(i) IN GENERAL.—The registrations of pesticides are to
be periodically reviewed.
(ii) REGULATIONS.—In accordance with this subparagraph, the Administrator shall by regulation establish a
procedure for accomplishing the periodic review of registrations.
(iii) INITIAL REGISTRATION REVIEW.—The Administrator shall complete the registration review of each pesticide or pesticide case, which may be composed of 1 or
more active ingredients and the products associated with
the active ingredients, not later than the later of—
(I) October 1, 2022; or
(II) the date that is 15 years after the date on
which the first pesticide containing a new active ingredient is registered.
(iv) SUBSEQUENT REGISTRATION REVIEW.—Not later
than 15 years after the date on which the initial registration review is completed under clause (iii) and each 15
years thereafter, the Administrator shall complete a subsequent registration review for each pesticide or pesticide
case.
(v) CANCELLATION.—No registration shall be canceled
as a result of the registration review process unless the
Administrator follows the procedures and substantive requirements of section 6.
(B) DOCKETING.—
(i) IN GENERAL.—Subject to clause (ii), after meeting
with 1 or more individuals that are not government employees to discuss matters relating to a registration review, the Administrator shall place in the docket minutes
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of the meeting, a list of attendees, and any documents exchanged at the meeting, not later than the earlier of—
(I) the date that is 45 days after the meeting; or
(II) the date of issuance of the registration review
decision.
(ii) PROTECTED INFORMATION.—The Administrator
shall identify, but not include in the docket, any confidential business information the disclosure of which is prohibited by section 10.
(C) LIMITATION.—Nothing in this subsection shall prohibit
the Administrator from undertaking any other review of a pesticide pursuant to this Act.
(2)(A) DATA.—The Administrator shall use the authority in
subsection (c)(2)(B) to require the submission of data when
such data are necessary for a registration review.
(B) DATA SUBMISSION, COMPENSATION, AND EXEMPTION.—
For purposes of this subsection, the provisions of subsections
(c)(1), (c)(2)(B), and (c)(2)(D) shall be utilized for and be applicable to any data required for registration review.
(h) REGISTRATION REQUIREMENTS FOR ANTIMICROBIAL PESTICIDES.—
(1) EVALUATION OF PROCESS.—To the maximum extent
practicable consistent with the degrees of risk presented by an
antimicrobial pesticide and the type of review appropriate to
evaluate the risks, the Administrator shall identify and evaluate reforms to the antimicrobial registration process that
would reduce review periods existing as of the date of enactment of this subsection [Aug. 3, 1996] for antimicrobial pesticide product registration applications and applications for
amended registration of antimicrobial pesticide products, including—
(A) new antimicrobial active ingredients;
(B) new antimicrobial end-use products;
(C) substantially similar or identical antimicrobial pesticides; and
(D) amendments to antimicrobial pesticide registrations.
(2) REVIEW TIME PERIOD REDUCTION GOAL.—Each reform
identified under paragraph (1) shall be designed to achieve the
goal of reducing the review period following submission of a
complete application, consistent with the degree of risk, to a
period of not more than—
(A) 540 days for a new antimicrobial active ingredient
pesticide registration;
(B) 270 days for a new antimicrobial use of a registered active ingredient;
(C) 120 days for any other new antimicrobial product;
(D) 90 days for a substantially similar or identical
antimicrobial product;
(E) 90 days for an amendment to an antimicrobial registration that does not require scientific review of data;
and
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(F) 120 days for an amendment to an antimicrobial
registration that requires scientific review of data and that
is not otherwise described in this paragraph.
(3) IMPLEMENTATION.—
(A) PROPOSED RULEMAKING.—
(i) ISSUANCE.—Not later than 270 days after the
date of enactment of this subsection [Aug. 3, 1996],
the Administrator shall publish in the Federal Register proposed regulations to accelerate and improve
the review of antimicrobial pesticide products designed
to implement, to the extent practicable, the goals set
forth in paragraph (2).
(ii) REQUIREMENTS.—Proposed regulations issued
under clause (i) shall—
(I) define the various classes of antimicrobial
use patterns, including household, industrial, and
institutional disinfectants and sanitizing pesticides, preservatives, water treatment, and pulp
and paper mill additives, and other such products
intended to disinfect, sanitize, reduce, or mitigate
growth or development of microbiological organisms, or protect inanimate objects, industrial
processes or systems, surfaces, water, or other
chemical substances from contamination, fouling,
or deterioration caused by bacteria, viruses, fungi,
protozoa, algae, or slime;
(II) differentiate the types of review undertaken for antimicrobial pesticides;
(III) conform the degree and type of review to
the risks and benefits presented by antimicrobial
pesticides and the function of review under this
Act, considering the use patterns of the product,
toxicity, expected exposure, and product type;
(IV) ensure that the registration process is
sufficient to maintain antimicrobial pesticide efficacy and that antimicrobial pesticide products
continue to meet product performance standards
and effectiveness levels for each type of label
claim made; and
(V) implement effective and reliable deadlines
for process management.
(iii) COMMENTS.—In developing the proposed regulations, the Administrator shall solicit the views from
registrants and other affected parties to maximize the
effectiveness of the rule development process.
(B) FINAL REGULATIONS.—
(i) ISSUANCE.—The Administrator shall issue final
regulations not later than 240 days after the close of
the comment period for the proposed regulations.
(ii) FAILURE TO MEET GOAL.—If a goal described in
paragraph (2) is not met by the final regulations, the
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ulations included instead, and identify future steps to
attain the goal.
(iii) REQUIREMENTS.—In issuing final regulations,
the Administrator shall—
(I) consider the establishment of a certification process for regulatory actions involving
risks that can be responsibly managed, consistent
with the degree of risk, in the most cost-efficient
manner;
(II) consider the establishment of a certification process by approved laboratories as an adjunct to the review process;
(III) use all appropriate and cost-effective review mechanisms, including—
(aa) expanded use of notification and nonnotification procedures;
(bb) revised procedures for application review; and
(cc) allocation of appropriate resources to
ensure streamlined management of antimicrobial pesticide registrations; and
(IV) clarify criteria for determination of the
completeness of an application.
(C) EXPEDITED REVIEW.—This subsection does not affect the requirements or extend the deadlines or review periods contained in subsection (c)(3).
(D) ALTERNATIVE REVIEW PERIODS.—If the final regulations to carry out this paragraph are not effective 630 days
after the date of enactment of this subsection [Aug. 3,
1996], until the final regulations become effective, the review period, beginning on the date of receipt by the Agency
of a complete application, shall be—
(i) 2 years for a new antimicrobial active ingredient pesticide registration;
(ii) 1 year for a new antimicrobial use of a registered active ingredient;
(iii) 180 days for any other new antimicrobial
product;
(iv) 90 days for a substantially similar or identical
antimicrobial product;
(v) 90 days for an amendment to an antimicrobial
registration that does not require scientific review of
data; and
(vi) 120 days for an amendment to an antimicrobial registration that requires scientific review of
data and that is not otherwise described in this subparagraph.
(E) WOOD PRESERVATIVES.—An application for the registration, or for an amendment to the registration, of a
wood preservative product for which a claim of pesticidal
activity listed in section 2(mm) is made (regardless of any
other pesticidal claim that is made with respect to the
product) shall be reviewed by the Administrator within the
same period as that established under this paragraph for
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an antimicrobial pesticide product application, consistent
with the degree of risk posed by the use of the wood preservative product, if the application requires the applicant
to satisfy the same data requirements as are required to
support an application for a wood preservative product
that is an antimicrobial pesticide.
(F) NOTIFICATION.—
(i) IN GENERAL.—Subject to clause (iii), the Administrator shall notify an applicant whether an application has been granted or denied not later than the
final day of the appropriate review period under this
paragraph, unless the applicant and the Administrator
agree to a later date.
(ii) FINAL DECISION.—If the Administrator fails to
notify an applicant within the period of time required
under clause (i), the failure shall be considered an
agency action unlawfully withheld or unreasonably delayed for purposes of judicial review under chapter 7
of title 5, United States Code.
(iii) EXEMPTION.—This subparagraph does not
apply to an application for an antimicrobial pesticide
that is filed under subsection (c)(3)(B) prior to 90 days
after the date of enactment of this subsection [Aug. 3,
1996].
(iv) LIMITATION.—Notwithstanding clause (ii), the
failure of the Administrator to notify an applicant for
an amendment to a registration for an antimicrobial
pesticide shall not be judicially reviewable in a Federal or State court if the amendment requires scientific review of data within—
(I) the time period specified in subparagraph
(D)(vi), in the absence of a final regulation under
subparagraph (B); or
(II) the time period specified in paragraph
(2)(F), if adopted in a final regulation under subparagraph (B).
(4) ANNUAL REPORT.—
(A) SUBMISSION.—Beginning on the date of enactment
of this subsection [Aug. 3, 1996] and ending on the date
that the goals under paragraph (2) are achieved, the Administrator shall, not later than March 1 of each year, prepare and submit an annual report to the Committee on Agriculture of the House of Representatives and the Committee on Agriculture, Nutrition, and Forestry of the Senate.
(B) REQUIREMENTS.—A report submitted under subparagraph (A) shall include a description of—
(i) measures taken to reduce the backlog of pending registration applications;
(ii) progress toward achieving reforms under this
subsection; and
(iii) recommendations to improve the activities of
the Agency pertaining to antimicrobial registrations.
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SEC. 4. ø7 U.S.C. 136a–1¿ REREGISTRATION OF REGISTERED PESTICIDES.

(a) GENERAL RULE.—The Administrator shall reregister, in accordance with this section, each registered pesticide containing any
active ingredient contained in any pesticide first registered before
November 1, 1984, except for any pesticide as to which the Administrator has determined, after November 1, 1984, and before the effective date of this section [December 24, 1988], that—
(1) there are no outstanding data requirements; and
(2) the requirements of section 3(c)(5) have been satisfied.
(b) REREGISTRATION PHASES.—Reregistrations of pesticides
under this section shall be carried out in the following phases:
(1) The first phase shall include the listing under subsection (c) of the active ingredients of the pesticides that will
be reregistered.
(2) The second phase shall include the submission to the
Administrator under subsection (d) of notices by registrants respecting their intention to seek reregistration, identification by
registrants of missing and inadequate data for such pesticides,
and commitments by registrants to replace such missing or inadequate data within the applicable time period.
(3) The third phase shall include submission to the Administrator by registrants of the information required under subsection (e).
(4) The fourth phase shall include an independent, initial
review by the Administrator under subsection (f) of submissions under phases two and three, identification of outstanding
data requirements, and the issuance, as necessary, of requests
for additional data.
(5) The fifth phase shall include the review by the Administrator under subsection (g) of data submitted for reregistration and appropriate regulatory action by the Administrator.
(c) PHASE ONE.—
(1) PRIORITY FOR REREGISTRATION.—For purposes of the reregistration of the pesticides described in subsection (a), the
Administrator shall list the active ingredients of pesticides and
shall give priority to, among others, active ingredients (other
than active ingredients for which registration standards have
been issued before the effective date of this section [December
24, 1988]) that—
(A) are in use on or in food or feed and may result in
postharvest residues;
(B) may result in residues of potential toxicological
concern in potable ground water, edible fish, or shellfish;
(C) have been determined by the Administrator before
the effective date of this section [December 24, 1988] to
have significant outstanding data requirements; or
(D) are used on crops, including in greenhouses and
nurseries, where worker exposure is most likely to occur.
(2) REREGISTRATION LISTS.—For purposes of reregistration
under this section, the Administrator shall by order—
(A) not later than 70 days after the effective date of
this section [December 24, 1988], list pesticide active in-

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gredients for which registration standards have been
issued before such effective date;
(B) not later than 4 months after such effective date,
list the first 150 pesticide active ingredients, as determined under paragraph (1);
(C) not later than 7 months after such effective date,
list the second 150 pesticide active ingredients, as determined under paragraph (1); and
(D) not later than 10 months after such effective date,
list the remainder of the pesticide active ingredients, as
determined under paragraph (1).
Each list shall be published in the Federal Register.
(3) JUDICIAL REVIEW.—The content of a list issued by the
Administrator under paragraph (2) shall not be subject to
judicial review.
(4) NOTICE TO REGISTRANTS.—On the publication of a list
of pesticide active ingredients under paragraph (2), the Administrator shall send by certified mail to the registrants of the
pesticides containing such active ingredients a notice of the
time by which the registrants are to notify the Administrator
under subsection (d) whether the registrants intend to seek or
not to seek reregistration of such pesticides.
(d) PHASE TWO.—
(1) IN GENERAL.—The registrant of a pesticide that contains an active ingredient listed under subparagraph (B), (C),
or (D) of subsection (c)(2) shall submit to the Administrator,
within the time period prescribed by paragraph (4), the notice
described in paragraph (2) and any information, commitment,
or offer described in paragraph (3).
(2) NOTICE OF INTENT TO SEEK OR NOT TO SEEK REREGISTRATION.—
(A) The registrant of a pesticide containing an active
ingredient listed under subparagraph (B), (C), or (D) of
subsection (c)(2) shall notify the Administrator by certified
mail whether the registrant intends to seek or does not intend to seek reregistration of the pesticide.
(B) If a registrant submits a notice under subparagraph (A) of an intention not to seek reregistration of a
pesticide, the Administrator shall publish a notice in the
Federal Register stating that such a notice has been submitted.
(3) MISSING OR INADEQUATE DATA.—Each registrant of a
pesticide that contains an active ingredient listed under subparagraph (B), (C), or (D) of subsection (c)(2) and for which the
registrant submitted a notice under paragraph (2) of an intention to seek reregistration of such pesticide shall submit to the
Administrator—
(A) in accordance with regulations issued by the Administrator under section 3, an identification of—
(i) all data that are required by regulation to support the registration of the pesticide with respect to
such active ingredient;
(ii) data that were submitted by the registrant
previously in support of the registration of the pesSeptember 28, 2012

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ticide that are inadequate to meet such regulations;
and
(iii) data identified under clause (i) that have not
been submitted to the Administrator; and
(B) either—
(i) a commitment to replace the data identified
under subparagraph (A)(ii) and submit the data identified under subparagraph (A)(iii) within the applicable
time period prescribed by paragraph (4)(B); or
(ii) an offer to share in the cost to be incurred by
a person who has made a commitment under clause (i)
to replace or submit the data and an offer to submit
to arbitration as described by section 3(c)(2)(B) with
regard to such cost sharing.
For purposes of a submission by a registrant under subparagraph (A)(ii), data are inadequate if the data are derived from
a study with respect to which the registrant is unable to make
the certification prescribed by subsection (e)(1)(G) that the registrant possesses or has access to the raw data used in or generated by such study. For purposes of a submission by a registrant under such subparagraph, data shall be considered to
be inadequate if the data are derived from a study submitted
before January 1, 1970, unless it is demonstrated to the satisfaction of the Administrator that such data should be considered to support the registration of the pesticide that is to be
reregistered.
(4) TIME PERIODS.—
(A) A submission under paragraph (2) or (3) shall be
made—
(i) in the case of a pesticide containing an active
ingredient listed under subsection (c)(2)(B), not later
than 3 months after the date of publication of the listing of such active ingredient;
(ii) in the case of a pesticide containing an active
ingredient listed under subsection (c)(2)(C), not later
than 3 months after the date of publication of the listing of such active ingredient; and
(iii) in the case of a pesticide containing an active
ingredient listed under subsection (c)(2)(D), not later
than 3 months after the date of publication of the listing of such active ingredient.
On application, the Administrator may extend a time period prescribed by this subparagraph if the Administrator
determines that factors beyond the control of the registrant prevent the registrant from complying with such
period.
(B) A registrant shall submit data in accordance with
a commitment entered into under paragraph (3)(B) within
a reasonable period of time, as determined by the Administrator, but not more than 48 months after the date the
registrant submitted the commitment. The Administrator,
on application of a registrant, may extend the period prescribed by the preceding sentence by no more than 2 years
if extraordinary circumstances beyond the control of the
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registrant prevent the registrant from submitting data
within such prescribed period. Upon application of a registrant, the Administrator shall, in the case of a minor use,
extend the deadline for the production of residue chemistry
data under this subparagraph for data required solely to
support that minor use until the final deadline for submission of data under this section for the other uses of the
pesticide established as of the date of enactment of the
Food Quality Protection Act of 1996 [Aug. 3, 1996] if—
(i) the data to support other uses of the pesticide
on a food are being provided;
(ii) the registrant, in submitting a request for such
an extension provides a schedule, including interim
dates to measure progress, to assure that the data production will be completed before the expiration of the
extension period;
(iii) the Administrator has determined that such
extension will not significantly delay the Administrator’s schedule for issuing a reregistration eligibility determination required under this section; and
(iv) the Administrator has determined that based
on existing data, such extension would not significantly increase the risk of any unreasonable adverse
effect on the environment. 4–1 If the Administrator
grants an extension under this subparagraph, the Administrator shall monitor the development of the data
and shall ensure that the registrant is meeting the
schedule for the production of the data. If the Administrator determines that the registrant is not meeting
or has not met the schedule for the production of such
data, the Administrator may proceed in accordance
with clause (iv) of section 3(c)(2)(B) or other provisions
of this section, as appropriate, regarding the continued
registration of the affected products with the minor
use and shall inform the public of such action. Notwithstanding the provisions of this subparagraph, the
Administrator may take action to modify or revoke the
extension under this subparagraph if the Administrator determines that the extension for the minor use
may cause an unreasonable adverse effect on the environment. In such circumstance, the Administrator
shall provide written notice to the registrant revoking
the extension of time for submission of data. Such
data shall instead be due in accordance with the date
then established by the Administrator for submission
of the data.
(5) CANCELLATION AND REMOVAL.—
(A) If the registrant of a pesticide does not submit a
notice under paragraph (2) or (3) within the time prescribed by paragraph (4)(A), the Administrator shall issue
a notice of intent to cancel the registration of such reg4–1 Indentation of the following sentences of this subparagraph is so in original (as added by
sec. 201(c)(2) of P.L. 104–170). Probably should be indented the same as flush matter of this
subparagraph.

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istrant for such pesticide and shall publish the notice in
the Federal Register and allow 60 days for the submission
of comments on the notice. On expiration of such 60 days,
the Administrator, by order and without a hearing, may
cancel the registration or take such other action, including
extension of applicable time periods, as may be necessary
to enable reregistration of such pesticide by another person.
(B)(i) If—
(I) no registrant of a pesticide containing an active
ingredient listed under subsection (c)(2) notifies the
Administrator under paragraph (2) that the registrant
intends to seek reregistration of any pesticide containing that active ingredient;
(II) no such registrant complies with paragraph
(3)(A); or
(III) no such registrant makes a commitment
under paragraph (3)(B) to replace or submit all data
described in clauses (ii) and (iii) of paragraph (3)(A);
the Administrator shall publish in the Federal Register a
notice of intent to remove the active ingredient from the
list established under subsection (c)(2) and a notice of intent to cancel the registrations of all pesticides containing
such active ingredient and shall provide 60 days for comment on such notice.
(ii) After the 60-day period has expired, the Administrator, by order, may cancel any such registration without
hearing, except that the Administrator shall not cancel a
registration under this subparagraph if—
(I) during the comment period a person acquires
the rights of the registrant in that registration;
(II) during the comment period that person furnishes a notice of intent to reregister the pesticide in
accordance with paragraph (2); and
(III) not later than 120 days after the publication
of the notice under this subparagraph, that person has
complied with paragraph (3) and the fee prescribed by
this section has been paid.
(6) SUSPENSIONS AND PENALTIES.—The Administrator shall
issue a notice of intent to suspend the registration of a pesticide in accordance with the procedures prescribed by section
3(c)(2)(B)(iv) if the Administrator determines that (A) progress
is insufficient to ensure the submission of the data required for
such pesticide under a commitment made under paragraph
(3)(B) within the time period prescribed by paragraph (4)(B) or
(B) the registrant has not submitted such data to the Administrator within such time period. If the registrant does not commit to support a specific minor use of the pesticide, but is supporting and providing data in a timely and adequate fashion
to support uses of the pesticide on a food, or if all uses of the
pesticide are nonfood uses and the registrant does not commit
to support a specific minor use of the pesticide but is supporting and providing data in a timely and adequate fashion
to support other nonfood uses of the pesticide, the AdminisSeptember 28, 2012

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trator, at the written request of the registrant, shall not take
any action pursuant to this paragraph in regard to such unsupported minor use until the final deadline established as of the
date of enactment of the Food Quality Protection Act of 1996
[Aug. 3, 1996], for the submission of data under this section for
the supported uses identified pursuant to this paragraph unless the Administrator determines that the absence of the data
is significant enough to cause human health or environmental
concerns. On such a determination the Administrator may
refuse the request for extension by the registrant. Upon receipt
of the request from the registrant, the Administrator shall publish in the Federal Register a notice of the receipt of the request and the effective date upon which the uses not being
supported will be voluntarily deleted from the registration pursuant to section 6(f)(1). If the Administrator grants an extension under this paragraph, the Administrator shall monitor the
development of the data for the uses being supported and shall
ensure that the registrant is meeting the schedule for the production of such data. If the Administrator determines that the
registrant is not meeting or has not met the schedule for the
production of such data, the Administrator may proceed in accordance with section 3(c)(2)(B)(iv) regarding the continued
registration of the affected products with the minor and other
uses and shall inform the public of such action in accordance
with section 6(f)(2). Notwithstanding this subparagraph, the
Administrator may deny, modify, or revoke the temporary extension under this paragraph if the Administrator determines
that the continuation of the minor use may cause an unreasonable adverse effect on the environment. In the event of modification or revocation, the Administrator shall provide, in writing, to the registrant a notice revoking the temporary extension and establish a new effective date by which the minor use
shall be deleted from the registration.
(e) PHASE THREE.—
(1) INFORMATION ABOUT STUDIES.—Each registrant of a
pesticide that contains an active ingredient listed under subparagraph (B), (C), or (D) of subsection (c)(2) who has submitted a notice under subsection (d)(2) of an intent to seek the
reregistration of such pesticide shall submit, in accordance
with the guidelines issued under paragraph (4), to the
Administrator—
(A) a summary of each study concerning the active ingredient previously submitted by the registrant in support
of the registration of a pesticide containing such active ingredient and considered by the registrant to be adequate
to meet the requirements of section 3 and the regulations
issued under such section;
(B) a summary of each study concerning the active ingredient previously submitted by the registrant in support
of the registration of a pesticide containing such active ingredient that may not comply with the requirements of
section 3 and the regulations issued under such section but
which the registrant asserts should be deemed to comply
with such requirements and regulations;
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(C) a reformat of the data from each study summarized under subparagraph (A) or (B) by the registrant concerning chronic dosing, oncogenicity, reproductive effects,
mutagenicity, neurotoxicity, teratogenicity, or residue
chemistry of the active ingredient that were submitted to
the Administrator before January 1, 1982;
(D) where data described in subparagraph (C) are not
required for the active ingredient by regulations issued
under section 3, a reformat of acute and subchronic dosing
data submitted by the registrant to the Administrator before January 1, 1982, that the registrant considers to be
adequate to meet the requirements of section 3 and the
regulations issued under such section;
(E) an identification of data that are required to be
submitted to the Administrator under section 6(a)(2) indicating an adverse effect of the pesticide;
(F) an identification of any other information available
that in the view of the registrant supports the registration;
(G) a certification that the registrant or the Administrator possesses or has access to the raw data used in or
generated by the studies that the registrant summarized
under subparagraph (A) or (B);
(H) either—
(i) a commitment to submit data to fill each outstanding data requirement identified by the registrant; or
(ii) an offer to share in the cost of developing such
data to be incurred by a person who has made a commitment under clause (i) to submit such data, and an
offer to submit to arbitration as described by section
3(c)(2)(B) with regard to such cost sharing; and
(I) evidence of compliance with section 3(c)(1)(D)(ii)
and regulations issued thereunder with regard to previously submitted data as if the registrant were now seeking the original registration of the pesticide.
A registrant who submits a certification under subparagraph
(G) that is false shall be considered to have violated this Act
and shall be subject to the penalties prescribed by section 14.
(2) TIME PERIODS.—
(A) The information required by paragraph (1) shall be
submitted to the Administrator—
(i) in the case of a pesticide containing an active
ingredient listed under subsection (c)(2)(B), not later
than 12 months after the date of publication of the
listing of such active ingredient;
(ii) in the case of a pesticide containing an active
ingredient listed under subsection (c)(2)(C), not later
than 12 months after the date of publication of the
listing of such active ingredient; and
(iii) in the case of a pesticide containing an active
ingredient listed under subsection (c)(2)(D), not later
than 12 months after the date of publication of the
listing of such active ingredient.
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(B) A registrant shall submit data in accordance with
a commitment entered into under paragraph (1)(H) within
a reasonable period of time, as determined by the Administrator, but not more than 48 months after the date the
registrant submitted the commitment under such paragraph. The Administrator, on application of a registrant,
may extend the period prescribed by the preceding sentence by no more than 2 years if extraordinary circumstances beyond the control of the registrant prevent
the registrant from submitting data within such prescribed
period. Upon application of a registrant, the Administrator
shall, in the case of a minor use, extend the deadline for
the production of residue chemistry data under this subparagraph for data required solely to support that minor
use until the final deadline for submission of data under
this section for the other uses of the pesticide established
as of the date of enactment of the Food Quality Protection
Act of 1996 [Aug. 3, 1996] if—
(i) the data to support other uses of the pesticide
on a food are being provided;
(ii) the registrant, in submitting a request for such
an extension provides a schedule, including interim
dates to measure progress, to assure that the data production will be completed before the expiration of the
extension period;
(iii) the Administrator has determined that such
extension will not significantly delay the Administrator’s schedule for issuing a reregistration eligibility determination required under this section; and
(iv) the Administrator has determined that based
on existing data, such extension would not significantly increase the risk of any unreasonable adverse
effect on the environment. 4–2 If the Administrator
grants an extension under this subparagraph, the Administrator shall monitor the development of the data
and shall ensure that the registrant is meeting the
schedule for the production of the data. If the Administrator determines that the registrant is not meeting
or has not met the schedule for the production of such
data, the Administrator may proceed in accordance
with clause (iv) of section 3(c)(2)(B) or other provisions
of this section, as appropriate, regarding the continued
registration of the affected products with the minor
use and shall inform the public of such action. Notwithstanding the provisions of this subparagraph, the
Administrator may take action to modify or revoke the
extension under this subparagraph if the Administrator determines that the extension for the minor use
may cause an unreasonable adverse effect on the environment. In such circumstance, the Administrator
shall provide written notice to the registrant revoking
4–2 Indentation of the following sentences of this subparagraph is so in original (as added by
sec. 201(c)(2) of P.L. 104–170). Probably should be indented the same as flush matter of this
subparagraph.

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the extension of time for submission of data. Such
data shall instead be due in accordance with the date
then established by the Administrator for submission
of the data.
(3) CANCELLATION.—
(A) If the registrant of a pesticide fails to submit the
information required by paragraph (1) within the time prescribed by paragraph (2), the Administrator, by order and
without hearing, shall cancel the registration of such pesticide. If the registrant does not commit to support a specific minor use of the pesticide, but is supporting and providing data in a timely and adequate fashion to support
uses of the pesticide on a food, or if all uses of the pesticide are nonfood uses and the registrant does not commit
to support a specific minor use of the pesticide but is supporting and providing data in a timely and adequate fashion to support other nonfood uses of the pesticide, the Administrator, at the written request of the registrant, shall
not take any action pursuant to this subparagraph in regard to such unsupported minor use until the final deadline established as of the date of enactment of the Food
Quality Protection Act of 1996 [Aug. 3, 1996], for the submission of data under this section for the supported uses
identified pursuant to this subparagraph unless the Administrator determines that the absence of the data is significant enough to cause human health or environmental
concerns. On the basis of such determination, the Administrator may refuse the request for extension by the registrant. Upon receipt of the request from the registrant,
the Administrator shall publish in the Federal Register a
notice of the receipt of the request and the effective date
upon which the uses not being supported will be voluntarily deleted from the registration pursuant to section
6(f)(1). If the Administrator grants an extension under this
subparagraph, the Administrator shall monitor the development of the data for the uses being supported and shall
ensure that the registrant is meeting the schedule for the
production of such data. If the Administrator determines
that the registrant is not meeting or has not met the
schedule for the production of such data, the Administrator may proceed in accordance with section 3(c)(2)(B)(iv)
regarding the continued registration of the affected products with the minor and other uses and shall inform the
public of such action in accordance with section 6(f)(2).
Notwithstanding this subparagraph, the Administrator
may deny, modify, or revoke the temporary extension
under this subparagraph if the Administrator determines
that the continuation of the minor use may cause an unreasonable adverse effect on the environment. In the event
of modification or revocation, the Administrator shall provide, in writing, to the registrant a notice revoking the
temporary extension and establish a new effective date by
which the minor use shall be deleted from the registration.
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(B)(i) If the registrant of a pesticide submits the information required by paragraph (1) within the time prescribed by paragraph (2) and such information does not
conform to the guidelines for submissions established by
the Administrator, the Administrator shall determine
whether the registrant made a good faith attempt to conform its submission to such guidelines.
(ii) If the Administrator determines that the registrant
made a good faith attempt to conform its submission to
such guidelines, the Administrator shall provide the registrant a reasonable period of time to make any necessary
changes or corrections.
(iii)(I) If the Administrator determines that the registrant did not make a good faith attempt to conform its
submission to such guidelines, the Administrator may
issue a notice of intent to cancel the registration. Such a
notice shall be sent to the registrant by certified mail.
(II) The registration shall be canceled without a hearing or further notice at the end of 30 days after receipt by
the registrant of the notice unless during that time a request for a hearing is made by the registrant.
(III) If a hearing is requested, a hearing shall be conducted under section 6(d), except that the only matter for
resolution at the hearing shall be whether the registrant
made a good faith attempt to conform its submission to
such guidelines. The hearing shall be held and a determination made within 75 days after receipt of a request for
hearing.
(4) GUIDELINES.—
(A) Not later than 1 year after the effective date of
this section [December 24, 1988], the Administrator, by
order, shall issue guidelines to be followed by registrants
in—
(i) summarizing studies;
(ii) reformatting studies;
(iii) identifying adverse information; and
(iv) identifying studies that have been submitted
previously that may not meet the requirements of section 3 or regulations issued under such section,
under paragraph (1).
(B) Guidelines issued under subparagraph (A) shall
not be subject to judicial review.
(5) MONITORING.—The Administrator shall monitor the
progress of registrants in acquiring and submitting the data
required under paragraph (1).
(f) PHASE FOUR.—
(1) INDEPENDENT REVIEW AND IDENTIFICATION OF OUTSTANDING DATA REQUIREMENTS.—
(A) The Administrator shall review the submissions of
all registrants of pesticides containing a particular active
ingredient under subsections (d)(3) and (e)(1) to determine
if such submissions identified all the data that are missing
or inadequate for such active ingredient. To assist the review of the Administrator under this subparagraph, the
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Administrator may require a registrant seeking reregistration to submit complete copies of studies summarized
under subsection (e)(1).
(B) The Administrator shall independently identify
and publish in the Federal Register the outstanding data
requirements for each active ingredient that is listed
under subparagraph (B), (C), or (D) of subsection (c)(2) and
that is contained in a pesticide to be reregistered under
this section. The Administrator, at the same time, shall
issue a notice under section 3(c)(2)(B) for the submission
of the additional data that are required to meet such requirements.
(2) TIME PERIODS.—
(A) The Administrator shall take the action required
by paragraph (1)—
(i) in the case of a pesticide containing an active
ingredient listed under subsection (c)(2)(B), not later
than 18 months after the date of the listing of such active ingredient;
(ii) in the case of a pesticide containing an active
ingredient listed under subsection (c)(2)(C), not later
than 24 months after the date of the listing of such active ingredient; and
(iii) in the case of a pesticide containing an active
ingredient listed under subsection (c)(2)(D), not later
than 33 months after the date of the listing of such active ingredient.
(B) If the Administrator issues a notice to a registrant
under paragraph (1)(B) for the submission of additional
data, the registrant shall submit such data within a reasonable period of time, as determined by the Administrator, but not to exceed 48 months after the issuance of
such notice. The Administrator, on application of a registrant, may extend the period prescribed by the preceding
sentence by no more than 2 years if extraordinary circumstances beyond the control of the registrant prevent
the registrant from submitting data within such prescribed
period. Upon application of a registrant, the Administrator
shall, in the case of a minor use, extend the deadline for
the production of residue chemistry data under this subparagraph for data required solely to support that minor
use until the final deadline for submission of data under
this section for the other uses of the pesticide established
as of the date of enactment of the Food Quality Protection
Act of 1996 [Aug. 3, 1996] if—
(i) the data to support other uses of the pesticide
on a food are being provided;
(ii) the registrant, in submitting a request for such
an extension provides a schedule, including interim
dates to measure progress, to assure that the data production will be completed before the expiration of the
extension period;
(iii) the Administrator has determined that such
extension will not significantly delay the AdministraSeptember 28, 2012

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tor’s schedule for issuing a reregistration eligibility determination required under this section; and
(iv) the Administrator has determined that based
on existing data, such extension would not significantly increase the risk of any unreasonable adverse
effect on the environment. 4–3 If the Administrator
grants an extension under this subparagraph, the Administrator shall monitor the development of the data
and shall ensure that the registrant is meeting the
schedule for the production of the data. If the Administrator determines that the registrant is not meeting
or has not met the schedule for the production of such
data, the Administrator may proceed in accordance
with clause (iv) of section 3(c)(2)(B) or other provisions
of this section, as appropriate, regarding the continued
registration of the affected products with the minor
use and shall inform the public of such action. Notwithstanding the provisions of this subparagraph, the
Administrator may take action to modify or revoke the
extension under this subparagraph if the Administrator determines that the extension for the minor use
may cause an unreasonable adverse effect on the environment. In such circumstance, the Administrator
shall provide written notice to the registrant revoking
the extension of time for submission of data. Such
data shall instead be due in accordance with the date
then established by the Administrator for submission
of the data.
(3) SUSPENSIONS AND PENALTIES.—The Administrator shall
issue a notice of intent to suspend the registration of a pesticide in accordance with the procedures prescribed by section
3(c)(2)(B)(iv) if the Administrator determines that (A) tests necessary to fill an outstanding data requirement for such pesticide have not been initiated within 1 year after the issuance
of a notice under paragraph (1)(B), or (B) progress is insufficient to ensure submission of the data referred to in clause (A)
within the time period prescribed by paragraph (2)(B) or the
required data have not been submitted to the Administrator
within such time period. If the registrant does not commit to
support a specific minor use of the pesticide, but is supporting
and providing data in a timely and adequate fashion to support
uses of the pesticide on a food, or if all uses of the pesticide
are nonfood uses and the registrant does not commit to support
a specific minor use of the pesticide but is supporting and providing data in a timely and adequate fashion to support other
nonfood uses of the pesticide, the Administrator, at the written
request of the registrant, shall not take any action pursuant to
this paragraph in regard to such unsupported minor use until
the final deadline established as of the date of enactment of
the Food Quality Protection Act of 1996 [Aug. 3, 1996], for the
submission of data under this section for the supported uses
4–3 Indentation of the following sentences of this subparagraph is so in original (as added by
sec. 201(c)(2) of P.L. 104–170). Probably should be indented the same as flush matter of this
subparagraph.

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identified pursuant to this paragraph unless the Administrator
determines that the absence of the data is significant enough
to cause human health or environmental concerns. On such a
determination the Administrator may refuse the request for extension by the registrant. Upon receipt of the request from the
registrant, the Administrator shall publish in the Federal Register a notice of the receipt of the request and the effective date
upon which the uses not being supported will be voluntarily
deleted from the registration pursuant to section 6(f)(1). If the
Administrator grants an extension under this paragraph, the
Administrator shall monitor the development of the data for
the uses being supported and shall ensure that the registrant
is meeting the schedule for the production of such data. If the
Administrator determines that the registrant is not meeting or
has not met the schedule for the production of such data, the
Administrator may proceed in accordance with section
3(c)(2)(B)(iv) regarding the continued registration of the affected products with the minor and other uses and shall inform
the public of such action in accordance with section 6(f)(2). Notwithstanding this subparagraph, the Administrator may deny,
modify, or revoke the temporary extension under this paragraph if the Administrator determines that the continuation of
the minor use may cause an unreasonable adverse effect on the
environment. In the event of modification or revocation, the
Administrator shall provide, in writing, to the registrant a notice revoking the temporary extension and establish a new effective date by which the minor use shall be deleted from the
registration.
(g) PHASE FIVE.—
(1) DATA REVIEW.—The Administrator shall conduct a thorough examination of all data submitted under this section concerning an active ingredient listed under subsection (c)(2) and
of all other available data found by the Administrator to be relevant.
(2) REREGISTRATION AND OTHER ACTIONS.—
(A) IN GENERAL.—The Administrator shall make a determination as to eligibility for reregistration—
(i) for all active ingredients subject to reregistration under this section for which tolerances or exemptions from tolerances are required under the Federal
Food, Drug, and Cosmetic Act (21 U.S.C. 301 et seq.),
not later than the last date for tolerance reassessment
established under section 408(q)(1)(C) of that Act (21
U.S.C. 346a(q)(1)(C)); and
(ii) for all other active ingredients subject to reregistration under this section, not later than October 3,
2008.
(B) PRODUCT-SPECIFIC DATA.—
(i) IN GENERAL.—Before reregistering a pesticide,
the Administrator shall obtain any needed productspecific data regarding the pesticide by use of section
3(c)(2)(B) and shall review such data within 90 days
after its submission.
(ii) TIMING.—
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(I) IN GENERAL.—Subject to subclause (II), the
Administrator shall require that data under this
subparagraph be submitted to the Administrator
not later than 8 months after a determination of
eligibility under subparagraph (A) has been made
for each active ingredient of the pesticide, unless
the Administrator determines that a longer period
is required for the generation of the data.
(II) EXTRAORDINARY CIRCUMSTANCES.—In the
case of extraordinary circumstances, the Administrator may provide such a longer period, of not
more than 2 additional years, for submission of
data to the Administrator under this subparagraph.
(C) After conducting the review required by paragraph
(1) for each active ingredient of a pesticide and the review
required by subparagraph (B) of this paragraph, the Administrator shall determine whether to reregister a pesticide by determining whether such pesticide meets the requirements of section 3(c)(5). If the Administrator determines that a pesticide is eligible to be reregistered, the Administrator shall reregister such pesticide within 6 months
after the submission of the data concerning such pesticide
under subparagraph (B).
(D) DETERMINATION TO NOT REREGISTER.—
(i) IN GENERAL.—If after conducting a review
under paragraph (1) or subparagraph (B) of this paragraph the Administrator determines that a pesticide
should not be reregistered, the Administrator shall
take appropriate regulatory action.
(ii) TIMING FOR REGULATORY ACTION.—Regulatory
action under clause (i) shall be completed as expeditiously as possible.
(E) As soon as the Administrator has sufficient information with respect to the dietary risk of a particular active ingredient, but in any event no later than the time the
Administrator makes a determination under subparagraph
(C) or (D) with respect to pesticides containing a particular
active ingredient, the Administrator shall—
(i) reassess each associated tolerance and exemption from the requirement for a tolerance issued under
section 408 of the Federal Food, Drug, and Cosmetic
Act (21 U.S.C. 346a);
(ii) determine whether such tolerance or exemption meets the requirements of that Act;
(iii) determine whether additional tolerances or
exemptions should be issued;
(iv) publish in the Federal Register a notice setting forth the determinations made under this subparagraph; and
(v) commence promptly such proceedings under
this Act and section 408 of the Federal Food, Drug,
and Cosmetic Act as are warranted by such determinations.
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(h) COMPENSATION OF DATA SUBMITTER.—If data that are submitted by a registrant under subsection (d), (e), (f), or (g) are used
to support the application of another person under section 3, the
registrant who submitted such data shall be entitled to compensation for the use of such data as prescribed by section 3(c)(1)(D). In
determining the amount of such compensation, the fees paid by the
registrant under this section shall be taken into account.
(i) FEES.—
(1) MAINTENANCE FEE.—
(A) IN GENERAL.—Subject to other provisions of this
paragraph, each registrant of a pesticide shall pay an annual fee by January 15 of each year for each registration,
except that no fee shall be charged for more than 200 registrations held by any registrant.
(B) In the case of a pesticide that is registered for a
minor agricultural use, the Administrator may reduce or
waive the payment of the fee imposed under this paragraph if the Administrator determines that the fee would
significantly reduce the availability of the pesticide for the
use.
(C) TOTAL AMOUNT OF FEES.—The amount of each fee
prescribed under subparagraph (A) shall be adjusted by
the Administrator to a level that will result in the collection under this paragraph of, to the extent practicable, an
aggregate amount of $27,800,000 for each of fiscal years
2013 through 2017.
(D) 4–4 MAXIMUM AMOUNT OF FEES FOR REGISTRANTS.—
The maximum annual fee payable under this paragraph
by—
(i) a registrant holding not more than 50 pesticide
registrations shall be $115,500 for each of fiscal years
2013 through 2017; and
(ii) a registrant holding over 50 registrations shall
be $184,800 for each of fiscal years 2013 through 2017.
(E) MAXIMUM AMOUNT OF FEES FOR SMALL BUSINESSES.—
(i) IN GENERAL.—For a small business, the maximum annual fee payable under this paragraph by—
(I) a registrant holding not more than 50 pesticide registrations shall be $70,600 for each of fiscal years 2013 through 2017; and
(II) a registrant holding over 50 pesticide registrations shall be $122,100 for each of fiscal years
2013 through 2017.
(ii) DEFINITION OF SMALL BUSINESS.—
(I) IN GENERAL.—In clause (i), the term ‘‘small
business’’ means a corporation, partnership, or unincorporated business that—
4–4 Title II of the Emergency Wartime Supplemental Appropriations Act, 2003, P.L. 108–11,
117 Stat. 603, provided that ‘‘Within 30 days of enactment of this Act, the Administrator of the
Environmental Protection Agency shall adjust each ‘maximum annual fee payable’ pursuant to
7 U.S.C. 136a–1(i)(5)(D) and (E) in a manner such that maintenance fee collections made to
reach the level authorized in division K of Public Law 108–7 shall be established in the same
proportion as those maintenance fee collections authorized in Public Law 107–73.’’.

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(aa) has 500 or fewer employees; and
(bb) during the 3-year period prior to the
most recent maintenance fee billing cycle, had
an average annual global gross revenue from
pesticides that did not exceed $60,000,000.
(II) AFFILIATES.—
(aa) IN GENERAL.—In the case of a business entity with 1 or more affiliates, the gross
revenue limit under subclause (I)(bb) shall
apply to the gross revenue for the entity and
all of the affiliates of the entity, including
parents and subsidiaries, if applicable.
(bb) AFFILIATED PERSONS.—For the purpose of item (aa), persons are affiliates of each
other if, directly or indirectly, either person
controls or has the power to control the other
person, or a third person controls or has the
power to control both persons.
(cc) INDICIA OF CONTROL.—For the purpose of item (aa), indicia of control include
interlocking management or ownership, identity of interests among family members,
shared facilities and equipment, and common
use of employees.
(F) FEE REDUCTION FOR CERTAIN SMALL BUSINESSES.—
(i) DEFINITION.—In this subparagraph, the term
‘‘qualified small business entity’’ means a corporation,
partnership, or unincorporated business that—
(I) has 500 or fewer employees;
(II) during the 3-year period prior to the most
recent maintenance fee billing cycle, had an average annual global gross revenue from all sources
that did not exceed $10,000,000; and
(III) holds not more than 5 pesticide registrations under this paragraph.
(ii) WAIVER.—Except as provided in clause (iii),
the Administrator shall waive 25 percent of the fee
under this paragraph applicable to the first registration of any qualified small business entity under this
paragraph.
(iii) LIMITATION.—The Administrator shall not
grant a waiver under clause (ii) to a qualified small
business entity if the Administrator determines that
the entity has been formed or manipulated primarily
for the purpose of qualifying for the waiver.
(G) The Administrator shall exempt any public health
pesticide from the payment of the fee prescribed under this
paragraph if, in consultation with the Secretary of Health
and Human Services, the Administrator determines, based
on information supplied by the registrant, that the economic return to the registrant from sales of the pesticide
does not support the registration or reregistration of the
pesticide.
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(H) If any fee prescribed by this paragraph with respect to the registration of a pesticide is not paid by a registrant by the time prescribed, the Administrator, by order
and without hearing, may cancel the registration.
(I) The authority provided under this paragraph shall
terminate on September 30, 2017.
(2) OTHER FEES.—Except as provided in section 33, during
the period beginning on the date of enactment of this section
[October 25, 1988] and ending on September 30, 2019, the Administrator may not levy any other fees for the registration of
a pesticide under this Act except as provided in paragraph (1).
(j) EXEMPTION OF CERTAIN REGISTRANTS.—The requirements of
subsections (d), (e), (f), and (i) (other than subsection (i)(1)) regarding data concerning an active ingredient and fees for review of such
data shall not apply to any person who is the registrant of a pesticide to the extent that, under section 3(c)(2)(D), the person would
not be required to submit or cite such data to obtain an initial registration of such pesticide.
(k) REREGISTRATION AND EXPEDITED PROCESSING FUND.—
(1) ESTABLISHMENT.—There shall be established in the
Treasury of the United States a reregistration and expedited
processing fund which shall be known as the Reregistration
and Expedited Processing Fund. 4–5
(2) 4–6 SOURCE AND USE.—
(A) All moneys derived from fees collected by the Administrator under subsection (i) shall be deposited in the
fund and shall be available to the Administrator, without
fiscal year limitation, specifically to offset the costs of reregistration and expedited processing of the applications
specified in paragraph (3), to enhance the information systems capabilities to improve the tracking of pesticide registration decisions, and to offset the costs of registration
review under section 3(g). Such moneys derived from fees
may not be expended in any fiscal year to the extent such
moneys derived from fees would exceed money appropriated for use by the Administrator and expended in such
year for such costs of reregistration and expedited processing of such applications. The Administrator shall, prior
to expending any such moneys derived from fees—
(i) effective October 1, 1997, adopt specific and
cost accounting rules and procedures as approved by
the General Accounting Office [General Accountability
Office] and the Inspector General of the Environmental Protection Agency to ensure that moneys derived from fees are allocated solely to the costs of reregistration and expedited processing of the applications specified in paragraph (3), to enhance the information systems capabilities to improve the tracking of
4–5 Sec. 501(b) of P.L. 104–170 amended sec. 4(k)(1) (7 U.S.C. 136a–1(k)(1)) by inserting ‘‘which
shall be known as the Reregistration and Expedited Processing Fund’’, without specifying the
Act that was being amended. The amendment was executed to this Act to effectuate the probable intent of Congress.
4–6 Sec. 501(c) of P.L. 104–170 amended sec. 4(k)(2) (7 U.S.C. 136a–1(k)(2)) to read as provided
above, without specifying the Act that was being amended. The amendment was executed to this
Act to effectuate the probable intent of Congress.

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pesticide registration decisions, and to offset the costs
of registration review under section 3(g);
(ii) prohibit the use of such moneys derived from
fees to pay for any costs other than those necessary to
achieve reregistration and expedited processing of the
applications specified in paragraph (3), to enhance the
information systems capabilities to improve the tracking of pesticide registration decisions, and to offset the
costs of registration review under section 3(g); and
(iii) ensure that personnel and facility costs associated with the functions to be carried out under this
paragraph do not exceed agency averages for comparable personnel and facility costs.
(B) The Administrator shall also—
(i) complete the review of unreviewed reregistration studies required to support the reregistration eligibility decisions scheduled for completion in accordance with subsection (l)(2); and
(ii) contract for such outside assistance as may be
necessary for review of required studies, using a generally accepted competitive process for the selection of
vendors of such assistance.
(3) REVIEW OF INERT INGREDIENTS; EXPEDITED PROCESSING
SIMILAR APPLICATIONS.—
(A) The Administrator shall use for each of the fiscal
years 2004 through 2006, approximately $3,300,000, and
for each of fiscal years 2013 through 2017, between 1⁄9 and
1⁄8, of the maintenance fees collected in such fiscal year 4–7
to obtain sufficient personnel and resources—
(i) to review and evaluate inert ingredients; and
(ii) to ensure the expedited processing and review
of any application that—
(I) proposes the initial or amended registration of an end-use pesticide that, if registered as
proposed, would be identical or substantially similar in composition and labeling to a currently-registered pesticide identified in the application, or
that would differ in composition and labeling from
any such currently-registered pesticide only in
ways that would not significantly increase the risk
of unreasonable adverse effects on the environment;
(II) proposes an amendment to the registration of a registered pesticide that does not require
scientific review of data; or
(III) proposes the initial or amended registration of an end use pesticide that, if registered as

4–7 P.L. 107–73 (115 Stat. 686) amended sec. 4(k)(3)(A) by striking ‘‘2001’’ and inserting ‘‘2002’’;
and by striking ‘‘1⁄7’’ and inserting ‘‘1⁄10’’. In an earlier enactment, sec. 501(d)(1) of P.L. 104–170
amended sec. 4(k)(3) (7 U.S.C. 136a–1(k)(3)) by striking ‘‘for each of the fiscal years 1992, 1993,
and 1994, 1⁄7th of the maintenance fees collected, up to 2 million each year’’ and inserting ‘‘for
each of the fiscal years 1997 through 2001, not more than 1⁄7 of the maintenance fees collected
in such fiscal year’’, without specifying the Act that was being amended and without including
a $ before ‘‘2 million’’. The earlier amendment was executed to this Act, and to strike ‘‘$2 million’’, to effectuate the probable intent of Congress.

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proposed, would be used for a public health pesticide.
(B) Any amounts made available under subparagraph
(A) shall be used to obtain sufficient personnel and resources to carry out the activities described in such subparagraph that are in addition to the personnel and resources available to carry out such activities on the date
of enactment of this section [October 25, 1988].
(C) 4–8 So long as the Administrator has not met the
time frames specified in clause (ii) of section 3(c)(3)(B) with
respect to any application subject to section 3(c)(3)(B) that
was received prior to the date of enactment of the Food
Quality Protection Act of 1996 [Aug. 3, 1996], the Administrator shall use the full amount of the fees specified in
subparagraph (A) for the purposes specified therein. Once
all applications subject to section 3(c)(3)(B) that were received prior to such date of enactment have been acted
upon, no limitation shall be imposed by the preceding sentence of this subparagraph so long as the Administrator
meets the time frames specified in clause (ii) of section
3(c)(3)(B) on 90 percent of affected applications in a fiscal
year. Should the Administrator not meet such time frames
in a fiscal year, the limitations imposed by the first sentence of this subparagraph shall apply until all overdue
applications subject to section 3(c)(3)(B) have been acted
upon.
(4) ENHANCEMENTS OF INFORMATION TECHNOLOGY SYSTEMS
FOR IMPROVEMENT IN REVIEW OF PESTICIDE APPLICATIONS.—
(A) IN GENERAL.—For each of fiscal years 2013
through 2017, the Administrator shall use not more than
$800,000 of the amounts made available to the Administrator in the Reregistration and Expedited Processing
Fund for the activities described in subparagraph (B).
(B) ACTIVITIES.—The Administrator shall use amounts
made available from the Reregistration and Expedited
Processing Fund to improve the information systems capabilities for the Office of Pesticide Programs to enhance
tracking of pesticide registration decisions, which shall include—
(i) the electronic tracking of—
(I) registration submissions; and
(II) the status of conditional registrations;
(ii) enhancing the database for information regarding endangered species assessments for registration review;
(iii) implementing the capability to electronically
review labels submitted with registration actions; and
(iv) acquiring and implementing the capability to
electronically assess and evaluate confidential statements of formula submitted with registration actions.
4–8 Sec. 501(d)(2) of P.L. 104–170 added subpara. (C) to sec. 4(k)(3) (7 U.S.C. 136a–1(k)(3)),
without specifying the Act that was being amended. The amendment was executed to this Act
to effectuate the probable intent of Congress.

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(5) UNUSED FUNDS.—Money in the fund not currently
needed to carry out this section shall be—
(A) maintained on hand or on deposit;
(B) invested in obligations of the United States or
guaranteed thereby; or
(C) invested in obligations, participations, or other instruments that are lawful investments for fiduciary, trust,
or public funds.
(6) 4–9 ACCOUNTING AND PERFORMANCE.—The Administrator shall take all steps necessary to ensure that expenditures from fees authorized by subsection (i)(1)(C)(ii) are used
only for the purposes described in paragraphs (2), (3), and (4)
and to carry out the goals established under subsection (l). The
Reregistration and Expedited Processing Fund shall be designated as an Environmental Protection Agency component for
purposes of section 3515(c) of title 31, United States Code. The
annual audit required under section 3521 of such title of the
financial statements of activities under this Act under section
3515(b) of such title shall include an audit of the fees collected
under subsection (i)(1)(C) and disbursed, of the amount appropriated to match such fees, and of the Administrator’s attainment of performance measures and goals established under
subsection (l). Such an audit shall also include a review of the
reasonableness of the overhead allocation and adequacy of disclosures of direct and indirect costs associated with carrying
out the reregistration and expedited processing of the applications specified in paragraph (3), and the basis for and accuracy
of all costs paid with moneys derived from such fees. The Inspector General shall conduct the annual audit and report the
findings and recommendations of such audit to the Administrator and to the Committees on Agriculture of the House of
Representatives and the Senate. The cost of such audit shall
be paid for out of the fees collected under subsection (i)(1)(C).
(l) 4–10 PERFORMANCE MEASURES AND GOAL.—The Administrator shall establish and publish annually in the Federal Register
performance measures and goals. Such measures and goals shall
include—
(1) the number of products reregistered, canceled, or
amended, the status of reregistration, the number and type of
data requests under section 3(c)(2)(B) issued to support product
reregistration by active ingredient, the progress in reducing
the number of unreviewed, required reregistration studies, the
aggregate status of tolerances reassessed, and the number of
applications for registration submitted under subsection (k)(3)
that were approved or disapproved;
(2) the future schedule for reregistrations, including the
projection for such schedules that will be issued under sub4–9 Sec. 501(e) of P.L. 104–170 amended sec. 4(k)(5) (7 U.S.C. 136a–1(k)(5)) to read as provided
above, without specifying the Act that was being amended. The amendment was executed to this
Act to effectuate the probable intent of Congress.
4–10 Sec. 501(f) of P.L. 104–170 amended sec. 4 (7 U.S.C. 136a–1) by redesignating subsecs.
(l) and (m) as subsecs. (m) and (n), respectively, and inserting a new subsec. (l), without specifying the Act that was being amended. The amendments were executed to this Act to effectuate
the probable intent of Congress.

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section (g)(2)(A) and (B) in the current fiscal year and the succeeding fiscal year; and
(3) the projected year of completion of the reregistrations
under this section.
(m) JUDICIAL REVIEW.—Any failure of the Administrator to
take any action required by this section shall be subject to judicial
review under the procedures prescribed by section 16(b).
(n) AUTHORIZATION OF FUNDS TO DEVELOP PUBLIC HEALTH
DATA.—
(1) DEFINITION.—For the purposes of this section, ‘‘Secretary’’ means the Secretary of Health and Human Services,
acting through the Public Health Service.
(2) CONSULTATION.—In the case of a pesticide registered
for use in public health programs for vector control or for other
uses the Administrator determines to be human health protection uses, the Administrator shall, upon timely request by the
registrant or any other interested person, or on the Administrator’s own initiative may, consult with the Secretary prior to
taking final action to suspend registration under section
3(c)(2)(B)(iv), or cancel a registration under section 4, 6(e), or
6(f). In consultation with the Secretary, the Administrator
shall prescribe the form and content of requests under this section.
(3) BENEFITS TO SUPPORT FAMILY.—The Administrator,
after consulting with the Secretary, shall make a determination whether the potential benefits of continued use of the pesticide for public health or health protection purposes are of
such significance as to warrant a commitment by the Secretary
to conduct or to arrange for the conduct of the studies required
by the Administrator to support continued registration under
section 3 or reregistration under section 4.
(4) ADDITIONAL TIME.—If the Administrator determines
that such a commitment is warranted and in the public interest, the Administrator shall notify the Secretary and shall, to
the extent necessary, amend a notice issued under section
3(c)(2)(B) to specify additional reasonable time periods for submission of the data.
(5) ARRANGEMENTS.—The Secretary shall make such arrangements for the conduct of required studies as the Secretary finds necessary and appropriate to permit submission of
data in accordance with the time periods prescribed by the Administrator. Such arrangements may include Public Health
Service intramural research activities, grants, contracts, or cooperative agreements with academic, public health, or other organizations qualified by experience and training to conduct
such studies.
(6) SUPPORT.—The Secretary may provide for support of
the required studies using funds authorized to be appropriated
under this section, the Public Health Service Act, or other appropriate authorities. After a determination is made under
subsection (d), the Secretary shall notify the Committees on
Appropriations of the House of Representatives and the Senate
of the sums required to conduct the necessary studies.
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(7) AUTHORIZATION OF APPROPRIATIONS.—There is authorized to be appropriated to carry out the purposes of this section
$12,000,000 for fiscal year 1997, and such sums as may be necessary for succeeding fiscal years.
SEC. 5. ø7 U.S.C. 136c¿ EXPERIMENTAL USE PERMITS.

(a) ISSUANCE.—Any person may apply to the Administrator for
an experimental use permit for a pesticide. The Administrator shall
review the application. After completion of the review, but not later
than one hundred and twenty days after receipt of the application
and all required supporting data, the Administrator shall either
issue the permit or notify the applicant of the Administrator’s determination not to issue the permit and the reasons therefor. The
applicant may correct the application or request a waiver of the
conditions for such permit within thirty days of receipt by the applicant of such notification. The Administrator may issue an experimental use permit only if the Administrator determines that the
applicant needs such permit in order to accumulate information
necessary to register a pesticide under section 3 of this Act. An application for an experimental use permit may be filed at any time.
(b) TEMPORARY TOLERANCE LEVEL.—If the Administrator determines that the use of a pesticide may reasonably be expected to
result in any residue on or in food or feed, the Administrator may
establish a temporary tolerance level for the residue of the pesticide before issuing the experimental use permit.
(c) USE UNDER PERMIT.—Use of a pesticide under an experimental use permit shall be under the supervision of the Administrator, and shall be subject to such terms and conditions and be for
such period of time as the Administrator may prescribe in the permit.
(d) STUDIES.—When any experimental use permit is issued for
a pesticide containing any chemical or combination of chemicals
which has not been included in any previously registered pesticide,
the Administrator may specify that studies be conducted to detect
whether the use of the pesticide under the permit may cause unreasonable adverse effects on the environment. All results of such
studies shall be reported to the Administrator before such pesticide
may be registered under section 3.
(e) REVOCATION.—The Administrator may revoke any experimental use permit, at any time, if the Administrator finds that its
terms or conditions are being violated, or that its terms and conditions are inadequate to avoid unreasonable adverse effects on the
environment.
(f) STATE ISSUANCE OF PERMITS.—Notwithstanding the foregoing provisions of this section, the Administrator shall, under
such terms and conditions as the Administrator may by regulations
prescribe, authorize any State to issue an experimental use permit
for a pesticide. All provisions of section 11 relating to State plans
shall apply with equal force to a State plan for the issuance of experimental use permits under this section.
(g) EXEMPTION FOR AGRICULTURAL RESEARCH AGENCIES.—Notwithstanding the foregoing provisions of this section, the Administrator may issue an experimental use permit for a pesticide to any
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tution which applies for such permit. Each permit shall not exceed
more than a one-year period or such other specific time as the Administrator may prescribe. Such permit shall be issued under such
terms and conditions restricting the use of the pesticide as the Administrator may require. Such pesticide may be used only by such
research agency or educational institution for purposes of experimentation.
SEC. 6. ø7 U.S.C. 136d¿ ADMINISTRATIVE REVIEW; SUSPENSION.

(a) EXISTING STOCKS AND INFORMATION.— 6–1
(1) EXISTING STOCKS.—The Administrator may permit the
continued sale and use of existing stocks of a pesticide whose
registration is suspended or canceled under this section, or section 3 or 4, to such extent, under such conditions, and for such
uses as the Administrator determines that such sale or use is
not inconsistent with the purposes of this Act.
(2) INFORMATION.—If at any time after the registration of
a pesticide the registrant has additional factual information regarding unreasonable adverse effects on the environment of
the pesticide, the registrant shall submit such information to
the Administrator.
(b) CANCELLATION AND CHANGE IN CLASSIFICATION.—If it appears to the Administrator that a pesticide or its labeling or other
material required to be submitted does not comply with the provisions of this Act or, when used in accordance with widespread and
commonly recognized practice, generally causes unreasonable adverse effects on the environment, the Administrator may issue a
notice of the Administrator’s intent either—
(1) to cancel its registration or to change its classification
together with the reasons (including the factual basis) for the
Administrator’s action, or
(2) to hold a hearing to determine whether or not its registration should be canceled or its classification changed.
Such notice shall be sent to the registrant and made public. In determining whether to issue any such notice, the Administrator
shall include among those factors to be taken into account the impact of the action proposed in such notice on production and prices
of agricultural commodities, retail food prices, and otherwise on the
agricultural economy. At least 60 days prior to sending such notice
to the registrant or making public such notice, whichever occurs
first, the Administrator shall provide the Secretary of Agriculture
with a copy of such notice and an analysis of such impact on the
agricultural economy. If the Secretary comments in writing to the
Administrator regarding the notice and analysis within 30 days
after receiving them, the Administrator shall publish in the Federal Register (with the notice) the comments of the Secretary and
the response of the Administrator with regard to the Secretary’s
comments. If the Secretary does not comment in writing to the Administrator regarding the notice and analysis within 30 days after
receiving them, the Administrator may notify the registrant and
make public the notice at any time after such 30-day period not-

6–1 Sec. 106(a)(1) of P.L. 104–170 amended subsec. (a) by striking the heading and inserting
‘‘(a) EXISTING STOCKS AND INFORMATION.—’’. The second subsec. designation for ‘‘(a)’’ was omitted to effectuate the probable intent of Congress.

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withstanding the foregoing 60-day time requirement. The time requirements imposed by the preceding 3 sentences may be waived
or modified to the extent agreed upon by the Administrator and the
Secretary. Notwithstanding any other provision of this subsection
(b) and section 25(d), in the event that the Administrator determines that suspension of a pesticide registration is necessary to
prevent an imminent hazard to human health, then upon such a
finding the Administrator may waive the requirement of notice to
and consultation with the Secretary of Agriculture pursuant to subsection (b) and of submission to the Scientific Advisory Panel pursuant to section 25(d) and proceed in accordance with subsection
(c). When a public health use is affected, the Secretary of Health
and Human Services should provide available benefits and use information, or an analysis thereof, in accordance with the procedures followed and subject to the same conditions as the Secretary
of Agriculture in the case of agricultural pesticides. The proposed
action shall become final and effective at the end of 30 days from
receipt by the registrant, or publication, of a notice issued under
paragraph (1), whichever occurs later, unless within that time either (i) the registrant makes the necessary corrections, if possible,
or (ii) a request for a hearing is made by a person adversely affected by the notice. In the event a hearing is held pursuant to
such a request or to the Administrator’s determination under paragraph (2), a decision pertaining to registration or classification
issued after completion of such hearing shall be final. In taking any
final action under this subsection, the Administrator shall consider
restricting a pesticide’s use or uses as an alternative to cancellation
and shall fully explain the reasons for these restrictions, and shall
include among those factors to be taken into account the impact of
such final action on production and prices of agricultural commodities, retail food prices, and otherwise on the agricultural economy,
and the Administrator shall publish in the Federal Register an
analysis of such impact.
(c) SUSPENSION.—
(1) ORDER.—If the Administrator determines that action is
necessary to prevent an imminent hazard during the time required for cancellation or change in classification proceedings,
the Administrator may, by order, suspend the registration of
the pesticide immediately. Except as provided in paragraph (3),
no order of suspension may be issued under this subsection unless the Administrator has issued, or at the same time issues,
a notice of intention to cancel the registration or change the
classification of the pesticide under subsection (b). Except as
provided in paragraph (3), the Administrator shall notify the
registrant prior to issuing any suspension order. Such notice
shall include findings pertaining to the question of ‘‘imminent
hazard’’. The registrant shall then have an opportunity, in accordance with the provisions of paragraph (2), for an expedited
hearing before the Administrator on the question of whether
an imminent hazard exists.
(2) EXPEDITE HEARING.—If no request for a hearing is submitted to the Administrator within five days of the registrant’s
receipt of the notification provided for by paragraph (1), the
suspension order may be issued and shall take effect and shall
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not be reviewable by a court. If a hearing is requested, it shall
commence within five days of the receipt of the request for
such hearing unless the registrant and the Administrator
agree that it shall commence at a later time. The hearing shall
be held in accordance with the provisions of subchapter II of
title 5 of the United States Code, except that the presiding officer need not be a certified hearing examiner. The presiding officer shall have ten days from the conclusion of the presentation of evidence to submit recommended findings and conclusions to the Administrator, who shall then have seven days to
render a final order on the issue of suspension.
(3) EMERGENCY ORDER.—Whenever the Administrator determines that an emergency exists that does not permit the
Administrator to hold a hearing before suspending, the Administrator may issue a suspension order in advance of notification
to the registrant. The Administrator may issue an emergency
order under this paragraph before issuing a notice of intention
to cancel the registration or change the classification of the
pesticide under subsection (b) and the Administrator shall proceed to issue the notice under subsection (b) within 90 days of
issuing an emergency order. If the Administrator does not
issue a notice under subsection (b) within 90 days of issuing
an emergency order, the emergency order shall expire. In the
case of an emergency order, paragraph (2) shall apply except
that (A) the order of suspension shall be in effect pending the
expeditious completion of the remedies provided by that paragraph and the issuance of a final order on suspension, and (B)
no party other than the registrant and the Administrator shall
participate except that any person adversely affected may file
briefs within the time allotted by the Administrator’s rules.
Any person so filing briefs shall be considered a party to such
proceeding for the purposes of section 16(b).
(4) JUDICIAL REVIEW.—A final order on the question of suspension following a hearing shall be reviewable in accordance
with Section 16 of this Act, notwithstanding the fact that any
related cancellation proceedings have not been completed. Any
order of suspension entered prior to a hearing before the Administrator shall be subject to immediate review in an action
by the registrant or other interested person with the concurrence of the registrant in an appropriate district court, solely
to determine whether the order of suspension was arbitrary,
capricious or an abuse of discretion, or whether the order was
issued in accordance with the procedures established by law.
The effect of any order of the court will be only to stay the effectiveness of the suspension order, pending the Administrator’s final decision with respect to cancellation or change in
classification. This action may be maintained simultaneously
with any administrative review proceeding under this section.
The commencement of proceedings under this paragraph shall
not operate as a stay of order, unless ordered by the court.
(d) PUBLIC HEARINGS AND SCIENTIFIC REVIEW.—In the event a
hearing is requested pursuant to subsection (b) or determined upon
by the Administrator pursuant to subsection (b), such hearing shall
be held after due notice for the purpose of receiving evidence relSeptember 28, 2012

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evant and material to the issues raised by the objections filed by
the applicant or other interested parties, or to the issues stated by
the Administrator, if the hearing is called by the Administrator
rather than by the filing of objections. Upon a showing of relevance
and reasonable scope of evidence sought by any party to a public
hearing, the Hearing Examiner shall issue a subpena to compel
testimony or production of documents from any person. The Hearing Examiner shall be guided by the principles of the Federal Rules
of Civil Procedure in making any order for the protection of the
witness or the content of documents produced and shall order the
payment of reasonable fees and expenses as a condition to requiring testimony of the witness. On contest, the subpena may be enforced by an appropriate United States district court in accordance
with the principles stated herein. Upon the request of any party to
a public hearing and when in the Hearing Examiner’s judgment it
is necessary or desirable, the Hearing Examiner shall at any time
before the hearing record is closed refer to a Committee of the National Academy of Sciences the relevant questions of scientific fact
involved in the public hearing. No member of any committee of the
National Academy of Sciences established to carry out the functions of this section shall have a financial or other conflict of interest with respect to any matter considered by such committee. The
Committee of the National Academy of Sciences shall report in
writing to the Hearing Examiner within 60 days after such referral
on these questions of scientific fact. The report shall be made public and shall be considered as part of the hearing record. The Administrator shall enter into appropriate arrangements with the National Academy of Sciences to assure an objective and competent
scientific review of the questions presented to Committees of the
Academy and to provide such other scientific advisory services as
may be required by the Administrator for carrying out the purposes
of this Act. As soon as practicable after completion of the hearing
(including the report of the Academy) but not later than 90 days
thereafter, the Administrator shall evaluate the data and reports
before the Administrator and issue an order either revoking the
Administrator’s notice of intention issued pursuant to this section,
or shall issue an order either canceling the registration, changing
the classification, denying the registration, or requiring modification of the labeling or packaging of the article. Such order shall be
based only on substantial evidence of record of such hearing and
shall set forth detailed findings of fact upon which the order is
based.
(e) CONDITIONAL REGISTRATION.—
(1) The Administrator shall issue a notice of intent to cancel a registration issued under section 3(c)(7) of this Act if (A)
the Administrator, at any time during the period provided for
satisfaction of any condition imposed, determines that the registrant has failed to initiate and pursue appropriate action toward fulfilling any condition imposed, or (B) at the end of the
period provided for satisfaction of any condition imposed, that
condition has not been met. The Administrator may permit the
continued sale and use of existing stocks of a pesticide whose
conditional registration has been canceled under this subsection to such extent, under such conditions, and for such uses
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as the Administrator may specify if the Administrator determines that such sale or use is not inconsistent with the purposes of this Act and will not have unreasonable adverse effects on the environment.
(2) A cancellation proposed under this subsection shall become final and effective at the end of thirty days from receipt
by the registrant of the notice of intent to cancel unless during
that time a request for hearing is made by a person adversely
affected by the notice. If a hearing is requested, a hearing shall
be conducted under subsection (d) of this section. The only
matters for resolution at that hearing shall be whether the registrant has initiated and pursued appropriate action to comply
with the condition or conditions within the time provided or
whether the condition or conditions have been satisfied within
the time provided, and whether the Administrator’s determination with respect to the disposition of existing stocks is consistent with this Act. A decision after completion of such hearing shall be final. Notwithstanding any other provision of this
section, a hearing shall be held and a determination made
within seventy-five days after receipt of a request for such
hearing.
(f) GENERAL PROVISIONS.—
(1) VOLUNTARY CANCELLATION.—
(A) A registrant may, at any time, request that a pesticide registration of the registrant be canceled or amended
to terminate one or more pesticide uses.
(B) Before acting on a request under subparagraph
(A), the Administrator shall publish in the Federal Register a notice of the receipt of the request and provide for
a 30-day period in which the public may comment.
(C) In the case of a pesticide that is registered for a
minor agricultural use, if the Administrator determines
that the cancellation or termination of uses would adversely affect the availability of the pesticide for use, the
Administrator—
(i) shall publish in the Federal Register a notice
of the receipt of the request and make reasonable efforts to inform persons who so use the pesticide of the
request; and
(ii) may not approve or reject the request until the
termination of the 180-day period beginning on the
date of publication of the notice in the Federal Register, except that the Administrator may waive the
180-day period upon the request of the registrant or if
the Administrator determines that the continued use
of the pesticide would pose an unreasonable adverse
effect on the environment.
(D) Subject to paragraph (3)(B), after complying with
this paragraph, the Administrator may approve or deny
the request.
(2) PUBLICATION OF NOTICE.—A notice of denial of registration, intent to cancel, suspension, or intent to suspend issued
under this Act or a notice issued under subsection (c)(4) or
(d)(5)(A) of section 4 shall be published in the Federal Register
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and shall be sent by certified mail, return receipt requested, to
the registrant’s or applicant’s address of record on file with the
Administrator. If the mailed notice is returned to the Administrator as undeliverable at that address, if delivery is refused,
or if the Administrator otherwise is unable to accomplish delivery of the notice to the registrant or applicant after making
reasonable efforts to do so, the notice shall be deemed to have
been received by the registrant or applicant on the date the notice was published in the Federal Register.
(3) TRANSFER OF REGISTRATION OF PESTICIDES REGISTERED
FOR MINOR AGRICULTURAL USES.—In the case of a pesticide that
is registered for a minor agricultural use:
(A) During the 180-day period referred to in paragraph
(1)(C)(ii), the registrant of the pesticide may notify the Administrator of an agreement between the registrant and a
person or persons (including persons who so use the pesticide) to transfer the registration of the pesticide, in lieu
of canceling or amending the registration to terminate the
use.
(B) An application for transfer of registration, in conformance with any regulations the Administrator may
adopt with respect to the transfer of the pesticide registrations, must be submitted to the Administrator within 30
days of the date of notification provided pursuant to subparagraph (A). If such an application is submitted, the Administrator shall approve the transfer and shall not approve the request for voluntary cancellation or amendment
to terminate use unless the Administrator determines that
the continued use of the pesticide would cause an unreasonable adverse effect on the environment.
(C) If the Administrator approves the transfer and the
registrant transfers the registration of the pesticide, the
Administrator shall not cancel or amend the registration
to delete the use or rescind the transfer of the registration,
during the 180-day period beginning on the date of the approval of the transfer unless the Administrator determines
that the continued use of the pesticide would cause an unreasonable adverse effect on the environment.
(D) The new registrant of the pesticide shall assume
the outstanding data and other requirements for the pesticide that are pending at the time of the transfer.
(4) UTILIZATION OF DATA FOR VOLUNTARILY CANCELED PESTICIDE.—When an application is filed with the Administrator
for the registration of a pesticide for a minor use and another
registrant subsequently voluntarily cancels its registration for
an identical or substantially similar pesticide for an identical
or substantially similar use, the Administrator shall process,
review, and evaluate the pending application as if the voluntary cancellation had not yet taken place except that the Administrator shall not take such action if the Administrator determines that such minor use may cause an unreasonable adverse effect on the environment. In order to rely on this subsection, the applicant must certify that it agrees to satisfy any
outstanding data requirements necessary to support the reregSeptember 28, 2012

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Sec. 7

istration of the pesticide in accordance with the data submission schedule established by the Administrator.
(g) NOTICE FOR STORED PESTICIDES WITH CANCELED OR SUSPENDED REGISTRATIONS.—
(1) IN GENERAL.—Any producer or exporter of pesticides,
registrant of a pesticide, applicant for registration of a pesticide, applicant for or holder of an experimental use permit,
commercial applicator, or any person who distributes or sells
any pesticide, who possesses any pesticide which has had its
registration canceled or suspended under this section shall notify the Administrator and appropriate State and local officials
of—
(A) such possession,
(B) the quantity of such pesticide such person possesses, and
(C) the place at which such pesticide is stored.
(2) COPIES.—The Administrator shall transmit a copy of
each notice submitted under this subsection to the regional office of the Environmental Protection Agency which has jurisdiction over the place of pesticide storage identified in the notice.
(h) JUDICIAL REVIEW.—Final orders of the Administrator under
this section shall be subject to judicial review pursuant to section
16.
SEC. 7. ø7 U.S.C. 136e¿ REGISTRATION OF ESTABLISHMENTS.

(a) REQUIREMENT.—No person shall produce any pesticide subject to this Act or active ingredient used in producing a pesticide
subject to this Act in any State unless the establishment in which
it is produced is registered with the Administrator. The application
for registration of any establishment shall include the name and
address of the establishment and of the producer who operates
such establishment.
(b) REGISTRATION.—Whenever the Administrator receives an
application under subsection (a), the Administrator shall register
the establishment and assign it an establishment number.
(c) INFORMATION REQUIRED.—
(1) Any producer operating an establishment registered
under this section shall inform the Administrator within 30
days after it is registered of the types and amounts of pesticides and, if applicable, active ingredients used in producing
pesticides—
(A) which the producer is currently producing;
(B) which the producer has produced during the past
year; and
(C) which the producer has sold or distributed during
the past year.
The information required by this paragraph shall be kept current and submitted to the Administrator annually as required
under such regulations as the Administrator may prescribe.
(2) Any such producer shall, upon the request of the Administrator for the purpose of issuing a stop sale order pursuant to section 13, inform the Administrator of the name and
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address of any recipient of any pesticide produced in any registered establishment which the producer operates.
(d) CONFIDENTIAL RECORDS AND INFORMATION.—Any information submitted to the Administrator pursuant to subsection (c)
other than the names of the pesticides or active ingredients used
in producing pesticides produced, sold, or distributed at an establishment shall be considered confidential and shall be subject to the
provisions of section 10.
SEC. 8. ø7 U.S.C. 136f¿ BOOKS AND RECORDS.

(a) REQUIREMENTS.—The Administrator may prescribe regulations requiring producers, registrants, and applicants for registration to maintain such records with respect to their operations and
the pesticides and devices produced as the Administrator determines are necessary for the effective enforcement of this Act and
to make the records available for inspection and copying in the
same manner as provided in subsection (b). No records required
under this subsection shall extend to financial data, sales data
other than shipment data, pricing data, personnel data, and research data (other than data relating to registered pesticides or to
a pesticide for which an application for registration has been filed).
(b) INSPECTION.—For the purposes of enforcing the provisions
of this Act, any producer, distributor, carrier, dealer, or any other
person who sells or offers for sale, delivers or offers for delivery any
pesticide or device subject to this Act, shall, upon request of any
officer or employee of the Environmental Protection Agency or of
any State or political subdivision, duly designated by the Administrator, furnish or permit such person at all reasonable times to
have access to, and to copy: (1) all records showing the delivery,
movement, or holding of such pesticide or device, including the
quantity, the date of shipment and receipt, and the name of the
consignor and consignee; or (2) in the event of the inability of any
person to produce records containing such information, all other
records and information relating to such delivery, movement, or
holding of the pesticide or device. Any inspection with respect to
any records and information referred to in this subsection shall not
extend to financial data, sales data other than shipment data, pricing data, personnel data, and research data (other than data relating to registered pesticides or to a pesticide for which an application for registration has been filed). Before undertaking an inspection under this subsection, the officer or employee must present to
the owner, operator, or agent in charge of the establishment or
other place where pesticides or devices are held for distribution or
sale, appropriate credentials and a written statement as to the reason for the inspection, including a statement as to whether a violation of the law is suspected. If no violation is suspected, an alternate and sufficient reason shall be given in writing. Each such inspection shall be commenced and completed with reasonable
promptness.
SEC. 9. ø7 U.S.C. 136g¿ INSPECTION OF ESTABLISHMENTS, ETC.

(a) IN GENERAL.—(1) For purposes of enforcing the provisions
of this Act, officers or employees of the Environmental Protection
Agency or of any State duly designated by the Administrator are
authorized to enter at reasonable times (A) any establishment or
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other place where pesticides or devices are held for distribution or
sale for the purpose of inspecting and obtaining samples of any pesticides or devices, packaged, labeled, and released for shipment,
and samples of any containers or labeling for such pesticides or devices, or (B) any place where there is being held any pesticide the
registration of which has been suspended or canceled for the purpose of determining compliance with section 19.
(2) Before undertaking such inspection, the officers or employees must present to the owner, operator, or agent in charge of the
establishment or other place where pesticides or devices are held
for distribution or sale, appropriate credentials and a written statement as to the reason for the inspection, including a statement as
to whether a violation of the law is suspected. If no violation is suspected, an alternate and sufficient reason shall be given in writing.
Each such inspection shall be commenced and completed with reasonable promptness. If the officer or employee obtains any samples,
prior to leaving the premises, the officer or employee shall give to
the owner, operator, or agent in charge a receipt describing the
samples obtained and, if requested, a portion of each such sample
equal in volume or weight to the portion retained. If an analysis
is made of such samples, a copy of the results of such analysis shall
be furnished promptly to the owner, operator, or agent in charge.
(b) WARRANTS.—For purposes of enforcing the provisions of
this Act and upon a showing to an officer or court of competent jurisdiction that there is reason to believe that the provisions of this
Act have been violated, officers or employees duly designated by
the Administrator are empowered to obtain and to execute warrants authorizing—
(1) entry, inspection, and copying of records for purposes of
this section or section 8;
(2) inspection and reproduction of all records showing the
quantity, date of shipment, and the name of consignor and consignee of any pesticide or device found in the establishment
which is adulterated, misbranded, not registered (in the case
of a pesticide) or otherwise in violation of this Act and in the
event of the inability of any person to produce records containing such information, all other records and information relating to such delivery, movement, or holding of the pesticide
or device; and
(3) the seizure of any pesticide or device which is in violation of this Act.
(c) ENFORCEMENT.—
(1) CERTIFICATION OF FACTS TO ATTORNEY GENERAL.—The
examination of pesticides or devices shall be made in the Environmental Protection Agency or elsewhere as the Administrator may designate for the purpose of determining from such
examinations whether they comply with the requirements of
this Act. If it shall appear from any such examination that
they fail to comply with the requirements of this Act, the Administrator shall cause notice to be given to the person against
whom criminal or civil proceedings are contemplated. Any person so notified shall be given an opportunity to present the
person’s views, either orally or in writing, with regard to such
contemplated proceedings, and if in the opinion of the AdminisSeptember 28, 2012

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trator it appears that the provisions of this Act have been violated by such person, then the Administrator shall certify the
facts to the Attorney General, with a copy of the results of the
analysis or the examination of such pesticide for the institution
of a criminal proceeding pursuant to section 14(b) or a civil
proceeding under section 14(a), when the Administrator determines that such action will be sufficient to effectuate the purposes of this Act.
(2) NOTICE NOT REQUIRED.—The notice of contemplated
proceedings and opportunity to present views set forth in this
subsection are not prerequisites to the institution of any proceeding by the Attorney General.
(3) WARNING NOTICES.—Nothing in this Act shall be construed as requiring the Administrator to institute proceedings
for prosecution of minor violations of this Act whenever the Administrator believes that the public interest will be adequately
served by a suitable written notice of warning.
SEC. 10. ø7 U.S.C. 136h¿ PROTECTION OF TRADE SECRETS AND OTHER
INFORMATION.

(a) IN GENERAL.—In submitting data required by this Act, the
applicant may (1) clearly mark any portions thereof which in the
applicant’s opinion are trade secrets or commercial or financial information and (2) submit such marked material separately from
other material required to be submitted under this Act.
(b) DISCLOSURE.—Notwithstanding any other provision of this
Act and subject to the limitations in subsections (d) and (e) of this
section, the Administrator shall not make public information which
in the Administrator’s judgment contains or relates to trade secrets
or commercial or financial information obtained from a person and
privileged or confidential, except that, when necessary to carry out
the provisions of this Act, information relating to formulas of products acquired by authorization of this Act may be revealed to any
Federal agency consulted and may be revealed at a public hearing
or in findings of fact issued by the Administrator.
(c) DISPUTES.—If the Administrator proposes to release for inspection information which the applicant or registrant believes to
be protected from disclosure under subsection (b), the Administrator shall notify the applicant or registrant, in writing, by certified mail. The Administrator shall not thereafter make available
for inspection such data until thirty days after receipt of the notice
by the applicant or registrant. During this period, the applicant or
registrant may institute an action in an appropriate district court
for a declaratory judgment as to whether such information is subject to protection under subsection (b).
(d) LIMITATIONS.—
(1) All information concerning the objectives, methodology,
results, or significance of any test or experiment performed on
or with a registered or previously registered pesticide or its
separate ingredients, impurities, or degradation products, and
any information concerning the effects of such pesticide on any
organism or the behavior of such pesticide in the environment,
including, but not limited to, data on safety to fish and wildlife,
humans and other mammals, plants, animals, and soil, and
studies on persistence, translocation and fate in the environ-

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ment, and metabolism, shall be available for disclosure to the
public. The use of such data for any registration purpose shall
be governed by section 3 of this Act. This paragraph does not
authorize the disclosure of any information that—
(A) discloses manufacturing or quality control processes,
(B) discloses the details of any methods for testing, detecting, or measuring the quantity of any deliberately
added inert ingredient of a pesticide, or
(C) discloses the identity or percentage quantity of any
deliberately added inert ingredient of a pesticide,
unless the Administrator has first determined that disclosure
is necessary to protect against an unreasonable risk of injury
to health or the environment.
(2) Information concerning production, distribution, sale,
or inventories of a pesticide that is otherwise entitled to confidential treatment under subsection (b) of this section may be
publicly disclosed in connection with a public proceeding to determine whether a pesticide, or any ingredient of a pesticide,
causes unreasonable adverse effects on health or the environment, if the Administrator determines that such disclosure is
necessary in the public interest.
(3) If the Administrator proposes to disclose information
described in clause (A), (B), or (C) of paragraph (1) or in paragraph (2) of this subsection, the Administrator shall notify by
certified mail the submitter of such information of the intent
to release such information. The Administrator may not release such information, without the submitter’s consent, until
thirty days after the submitter has been furnished such notice.
Where the Administrator finds that disclosure of information
described in clause (A), (B), or (C) of paragraph (1) of this subsection is necessary to avoid or lessen an imminent and substantial risk of injury to the public health, the Administrator
may set such shorter period of notice (but not less than ten
days) and such method of notice as the Administrator finds appropriate. During such period the data submitter may institute
an action in an appropriate district court to enjoin or limit the
proposed disclosure. The court may enjoin disclosure, or limit
the disclosure or the parties to whom disclosure shall be made,
to the extent that—
(A) in the case of information described in clause (A),
(B), or (C) of paragraph (1) of this subsection, the proposed
disclosure is not required to protect against an unreasonable risk of injury to health or the environment; or
(B) in the case of information described in paragraph
(2) of this subsection, the public interest in availability of
the information in the public proceeding does not outweigh
the interests in preserving the confidentiality of the information.
(e) DISCLOSURE TO CONTRACTORS.—Information otherwise protected from disclosure to the public under subsection (b) of this section may be disclosed to contractors with the United States and
employees of such contractors if, in the opinion of the Administrator, such disclosure is necessary for the satisfactory performance
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by the contractor of a contract with the United States for the performance of work in connection with this Act and under such conditions as the Administrator may specify. The Administrator shall require as a condition to the disclosure of information under this subsection that the person receiving it take such security precautions
respecting the information as the Administrator shall by regulation
prescribe.
(f) PENALTY FOR DISCLOSURE BY FEDERAL EMPLOYEES.—(1)
Any office or employee of the United States or former officer or employee of the United States who, by virtue of such employment or
official position, has obtained possession of, or has access to, material the disclosure of which is prohibited by subsection (b) of this
section, and who, knowing that disclosure of such material is prohibited by such subsection, willfully discloses the material in any
manner to any person not entitled to receive it, shall be fined not
more than $10,000 or imprisoned for not more than one year, or
both. Section 1905 of title 18 of the United States Code shall not
apply with respect to the publishing, divulging, disclosure, or making known of, or making available, information reported or otherwise obtained under this Act. Nothing in this Act shall preempt
any civil remedy under State or Federal law for wrongful disclosure
of trade secrets.
(2) For the purposes of this section, any contractor with the
United States who is furnished information as authorized by subsection (e) of this section, or any employee of any such contractor,
shall be considered to be an employee of the United States.
(g) DISCLOSURE TO FOREIGN AND MULTINATIONAL PESTICIDE
PRODUCERS.—(1) The Administrator shall not knowingly disclose
information submitted by an applicant or registrant under this Act
to any employee or agent of any business or other entity engaged
in the production, sale, or distribution of pesticides in countries
other than the United States or in addition to the United States
or to any other person who intends to deliver such data to such foreign or multinational business or entity unless the applicant or registrant has consented to such disclosure. The Administrator shall
require an affirmation from any person who intends to inspect data
that such person does not seek access to the data for purposes of
delivering it or offering it for sale to any such business or entity
or its agents or employees and will not purposefully deliver or negligently cause the data to be delivered to such business or entity
or its agents or employees. Notwithstanding any other provision of
this subsection, the Administrator may disclose information to any
person in connection with a public proceeding under law or regulation, subject to restrictions on the availability of information contained elsewhere in this Act, which information is relevant to a determination by the Administrator with respect to whether a pesticide, or any ingredient of a pesticide, causes unreasonable adverse
effects on health or the environment.
(2) The Administrator shall maintain records of the names of
persons to whom data are disclosed under this subsection and the
persons or organizations they represent and shall inform the applicant or registrant of the names and affiliations of such persons.
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(3) Section 1001 of title 18 of the United States Code shall
apply to any affirmation made under paragraph (1) of this subsection.
SEC. 11. ø7 U.S.C. 136i¿ USE OF RESTRICTED USE PESTICIDES; APPLICATORS.

(a) CERTIFICATION PROCEDURE.—
(1) FEDERAL CERTIFICATION.—In any State for which a
State plan for applicator certification has not been approved by
the Administrator, the Administrator, in consultation with the
Governor of such State, shall conduct a program for the certification of applicators of pesticides. Such program shall conform
to the requirements imposed upon the States under the provisions of subsection (a)(2) of this section and shall not require
private applicators to take any examination to establish competency in the use of pesticides. Prior to the implementation of
the program, the Administrator shall publish in the Federal
Register for review and comment a summary of the Federal
plan for applicator certification and shall make generally available within the State copies of the plan. The Administrator
shall hold public hearings at one or more locations within the
State if so requested by the Governor of such State during the
thirty days following publication of the Federal Register notice
inviting comment on the Federal plan. The hearings shall be
held within thirty days following receipt of the request from
the Governor. In any State in which the Administrator conducts a certification program, the Administrator may require
any person engaging in the commercial application, sale, offering for sale, holding for sale, or distribution of any pesticide
one or more uses of which have been classified for restricted
use to maintain such records and submit such reports concerning the commercial application, sale, or distribution of
such pesticide as the Administrator may be regulation prescribe. Subject to paragraph (2), the Administrator shall prescribe standards for the certification of applicators of pesticides. Such standards shall provide that to be certified, an individual must be determined to be competent with respect to
the use and handling of pesticides, or to the use and handling
of the pesticide or class of pesticides covered by such individual’s certification. The certification standard for a private applicator shall, under a State plan submitted for approval, be
deemed fulfilled by the applicator completing a certification
form. The Administrator shall further assure that such form
contains adequate information and affirmations to carry out
the intent of this Act, and may include in the form an affirmation that the private applicator has completed a training program approved by the Administrator so long as the program
does not require the private applicator to take, pursuant to a
requirement prescribed by the Administrator, any examination
to establish competency in the use of the pesticide. The Administrator may require any pesticide dealer participating in a certification program to be licensed under a State licensing program approved by the Administrator.
(2) STATE CERTIFICATION.—If any State, at any time, desires to certify applicators of pesticides, the Governor of such

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State shall submit a State plan for such purpose. The Administrator shall approve the plan submitted by any State, or any
modification thereof, if such plan in the Administrator’s judgment—
(A) designates a State agency as the agency responsible for administering the plan throughout the State;
(B) contains satisfactory assurances that such agency
has or will have the legal authority and qualified personnel necessary to carry out the plan;
(C) gives satisfactory assurances that the State will
devote adequate funds to the administration of the plan;
(D) provides that the State agency will make such reports to the Administrator in such form and containing
such information as the Administrator may from time to
time require; and
(E) contains satisfactory assurances that State standards for the certification of applicators of pesticides conform with those standards prescribed by the Administrator
under paragraph (1).
Any State certification program under this section shall be
maintained in accordance with the State plan approved under
this section.
(b) STATE PLANS.—If the Administrator rejects a plan submitted under subsection (a)(2), the Administrator shall afford the
State submitting the plan due notice and opportunity for hearing
before so doing. If the Administrator approves a plan submitted
under subsection (a)(2), then such State shall certify applicators of
pesticides with respect to such State. Whenever the Administrator
determines that a State is not administering the certification program in accordance with the plan approved under this section, the
Administrator shall so notify the State and provide for a hearing
at the request of the State, and, if appropriate corrective action is
not taken within a reasonable time, not to exceed ninety days, the
Administrator shall withdraw approval of such plan.
(c) INSTRUCTION IN INTEGRATED PEST MANAGEMENT TECHNIQUES.—Standards prescribed by the Administrator for the certification of applicators of pesticides under subsection (a), and the
State plans submitted to the Administrator under subsection (a),
shall include provisions for making instructional materials concerning integrated pest management techniques available to individuals at their request in accordance with the provisions of section
23(c) of this Act, but such plans may not require that any individual receive instruction concerning such techniques or be shown
to be competent with respect to the use of such techniques. The Administrator and States implementing such plans shall provide that
all interested individuals are notified of the availability of such instructional materials.
(d) IN GENERAL.—No regulations prescribed by the Administrator for carrying out the provisions of this Act shall require any
private applicator to maintain any records or file any reports or
other documents.
(e) SEPARATE STANDARDS.—When establishing or approving
standards for licensing or certification, the Administrator shall establish separate standards for commercial and private applicators.
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SEC. 12. ø7 U.S.C. 136j¿ UNLAWFUL ACTS.

Sec. 12

(a) IN GENERAL.—
(1) Except as provided by subsection (b), it shall be unlawful for any person in any State to distribute or sell to any person—
(A) any pesticide that is not registered under section
3 or whose registration has been canceled or suspended,
except to the extent that distribution or sale otherwise has
been authorized by the Administrator under this Act;
(B) any registered pesticide if any claims made for it
as a part of its distribution or sale substantially differ
from any claims made for it as a part of the statement required in connection with its registration under section 3;
(C) any registered pesticide the composition of which
differs at the time of its distribution or sale from its composition as described in the statement required in connection with its registration under section 3;
(D) any pesticide which has not been colored or discolored pursuant to the provisions of section 25(c)(5);
(E) any pesticide which is adulterated or misbranded;
or
(F) any device which is misbranded.
(2) It shall be unlawful for any person—
(A) to detach, alter, deface, or destroy, in whole or in
part, any labeling required under this Act;
(B) to refuse to—
(i) prepare, maintain, or submit any records required by or under section 5, 7, 8, 11, or 19;
(ii) submit any reports required by or under section 5, 6, 7, 8, 11, or 19; or
(iii) allow any entry, inspection, copying of
records, or sampling authorized by this Act;
(C) to give a guaranty or undertaking provided for in
subsection (b) which is false in any particular, except that
a person who receives and relies upon a guaranty authorized under subsection (b) may give a guaranty to the same
effect, which guaranty shall contain, in addition to the person’s own name and address, the name and address of the
person residing in the United States from whom the person received the guaranty or undertaking;
(D) to use for the person’s own advantage or to reveal,
other than to the Administrator, or officials or employees
of the Environmental Protection Agency or other Federal
executive agencies, or to the courts, or to physicians, pharmacists, and other qualified persons, needing such information for the performance of their duties, in accordance
with such directions as the Administrator may prescribe,
any information acquired by authority of this Act which is
confidential under this Act;
(E) who is a registrant, wholesaler, dealer, retailer, or
other distributor to advertise a product registered under
this Act for restricted use without giving the classification
of the product assigned to it under section 3;

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(F) to distribute or sell, or to make available for use,
or to use, any registered pesticide classified for restricted
use for some or all purposes other than in accordance with
section 3(d) and any regulations thereunder, except that it
shall not be unlawful to sell, under regulations issued by
the Administrator, a restricted use pesticide to a person
who is not a certified applicator for application by a certified applicator;
(G) to use any registered pesticide in a manner inconsistent with its labeling;
(H) to use any pesticide which is under an experimental use permit contrary to the provisions of such permit;
(I) to violate any order issued under section 13;
(J) to violate any suspension order issued under section 3(c)(2)(B), 4, or 6;
(K) to violate any cancellation order issued under this
Act or to fail to submit a notice in accordance with section
6(g);
(L) who is a producer to violate any of the provisions
of section 7;
(M) to knowingly falsify all or part of any application
for registration, application for experimental use permit,
any information submitted to the Administrator pursuant
to section 7, any records required to be maintained pursuant to this Act, any report filed under this Act, or any information marked as confidential and submitted to the Administrator under any provision of this Act;
(N) who is a registrant, wholesaler, dealer, retailer, or
other distributor to fail to file reports required by this Act;
(O) to add any substance to, or take any substance
from, any pesticide in a manner that may defeat the purpose of this Act;
(P) to use any pesticide in tests on human beings unless such human beings (i) are fully informed of the nature
and purposes of the test and of any physical and mental
health consequences which are reasonably foreseeable
therefrom, and (ii) freely volunteer to participate in the
test;
(Q) to falsify all or part of any information relating to
the testing of any pesticide (or any ingredient, metabolite,
or degradation product thereof), including the nature of
any protocol, procedure, substance, organism, or equipment used, observation made, or conclusion or opinion
formed, submitted to the Administrator, or that the person
knows will be furnished to the Administrator or will become a part of any records required to be maintained by
this Act;
(R) to submit to the Administrator data known to be
false in support of a registration; or
(S) to violate any regulation issued under section 3(a)
or 19.
(b) EXEMPTIONS.—The penalties provided for a violation of
paragraph (1) of subsection (a) shall not apply to—
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Sec. 13

(1) any person who establishes a guaranty signed by, and
containing the name and address of, the registrant or person
residing in the United States from whom the person purchased
or received in good faith the pesticide in the same unbroken
package, to the effect that the pesticide was lawfully registered
at the time of sale and delivery to the person, and that it complies with the other requirements of this Act, and in such case
the guarantor shall be subject to the penalties which would
otherwise attach to the person holding the guaranty under the
provisions of this Act;
(2) any carrier while lawfully shipping, transporting, or delivering for shipment any pesticide or device, if such carrier
upon request of any officer or employee duly designated by the
Administrator shall permit such officer or employee to copy all
of its records concerning such pesticide or device;
(3) any public official while engaged in the performance of
the official duties of the public official;
(4) any person using or possessing any pesticide as provided by an experimental use permit in effect with respect to
such pesticide and such use or possession; or
(5) any person who ships a substance or mixture of substances being put through tests in which the purpose is only
to determine its value for pesticide purposes or to determine its
toxicity or other properties and from which the user does not
expect to receive any benefit in pest control from its use.
SEC. 13. ø7 U.S.C. 136k¿ STOP SALE, USE, REMOVAL, AND SEIZURE.

(a) STOP SALE, ETC., ORDERS.—Whenever any pesticide or device is found by the Administrator in any State and there is reason
to believe on the basis of inspection or tests that such pesticide or
device is in violation of any of the provisions of this Act, or that
such pesticide or device has been or is intended to be distributed
or sold in violation of any such provisions, or when the registration
of the pesticide has been canceled by a final order or has been suspended, the Administrator may issue a written or printed ‘‘stop
sale, use, or removal’’ order to any person who owns, controls, or
has custody of such pesticide or device, and after receipt of such
order no person shall sell, use, or remove the pesticide or device described in the order except in accordance with the provisions of the
order.
(b) SEIZURE.—Any pesticide or device that is being transported
or, having been transported, remains unsold or in original unbroken packages, or that is sold or offered for sale in any State, or
that is imported from a foreign country, shall be liable to be proceeded against in any district court in the district where it is found
and seized for confiscation by a process in rem for condemnation
if—
(1) in the case of a pesticide—
(A) it is adulterated or misbranded;
(B) it is not registered pursuant to the provisions of
section 3;
(C) its labeling fails to bear the information required
by this Act;

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(D) it is not colored or discolored and such coloring or
discoloring is required under this Act; or
(E) any of the claims made for it or any of the directions for its use differ in substance from the representations made in connection with its registration;
(2) in the case of a device, it is misbranded; or
(3) in the case of a pesticide or device, when used in accordance with the requirements imposed under this Act and as
directed by the labeling, it nevertheless causes unreasonable
adverse effects on the environment.
In the case of a plant regulator, defoliant, or desiccant, used in accordance with the label claims and recommendations, physical or
physiological effects on plants or parts thereof shall not be deemed
to be injury, when such effects are the purpose for which the plant
regulator, defoliant, or desiccant was applied.
(c) DISPOSITION AFTER CONDEMNATION.—If the pesticide or device is condemned it shall, after entry of the decree, be disposed of
by destruction or sale as the court may direct and the proceeds, if
sold, less the court costs, shall be paid into the Treasury of the
United States, but the pesticide or device shall not be sold contrary
to the provisions of this Act or the laws of the jurisdiction in which
it is sold. On payment of the costs of the condemnation proceedings
and the execution and delivery of a good and sufficient bond conditioned that the pesticide or device shall not be sold or otherwise
disposed of contrary to the provisions of the Act or the laws of any
jurisdiction in which sold, the court may direct that such pesticide
or device be delivered to the owner thereof. The proceedings of such
condemnation cases shall conform, as near as may be to the proceedings in admiralty, except that either party may demand trial
by jury of any issue of fact joined in any case, and all such proceedings shall be at the suit of and in the name of the United
States.
(d) COURT COSTS, ETC.—When a decree of condemnation is entered against the pesticide or device, court costs and fees, storage,
and other proper expenses shall be awarded against the person, if
any, intervening as claimant of the pesticide or device.
SEC. 14. ø7 U.S.C. 136l¿ PENALTIES.

(a) CIVIL PENALTIES.—
(1) IN GENERAL.—Any registrant, commercial applicator,
wholesaler, dealer, retailer, or other distributor who violates
any provision of this Act may be assessed a civil penalty by the
Administrator of not more than $5,000 for each offense.
(2) PRIVATE APPLICATOR.—Any private applicator or other
person not included in paragraph (1) who violates any provision of this Act subsequent to receiving a written warning from
the Administrator or following a citation for a prior violation,
may be assessed a civil penalty by the Administrator of not
more than $1,000 for each offense, except that any applicator
not included under paragraph (1) of this subsection who holds
or applies registered pesticides, or uses dilutions of registered
pesticides, only to provide a service of controlling pests without
delivering any unapplied pesticide to any person so served, and
who violates any provision of this Act may be assessed a civil

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Sec. 15

penalty by the Administrator of not more than $500 for the
first offense nor more than $1,000 for each subsequent offense.
(3) HEARING.—No civil penalty shall be assessed unless the
person charged shall have been given notice and opportunity
for a hearing on such charge in the county, parish, or incorporated city of the residence of the person charged.
(4) DETERMINATION OF PENALTY.—In determining the
amount of the penalty, the Administrator shall consider the appropriateness of such penalty to the size of the business of the
person charged, the effect on the person’s ability to continue in
business, and the gravity of the violation. Whenever the Administrator finds that the violation occurred despite the exercise of due care or did not cause significant harm to health or
the environment, the Administrator may issue a warning in
lieu of assessing a penalty.
(5) REFERENCES TO ATTORNEY GENERAL.—In case of inability to collect such civil penalty or failure of any person to pay
all, or such portion of such civil penalty as the Administrator
may determine, the Administrator shall refer the matter to the
Attorney General, who shall recover such amount by action in
the appropriate United States district court.
(b) CRIMINAL PENALTIES.—
(1) IN GENERAL.—
(A) Any registrant, applicant for a registration, or producer who knowingly violates any provision of this Act
shall be fined not more than $50,000 or imprisoned for not
more than 1 year, or both.
(B) Any commercial applicator of a restricted use pesticide, or any other person not described in subparagraph
(A) who distributes or sells pesticides or devices, who
knowingly violates any provision of this Act shall be fined
not more than $25,000 or imprisoned for not more than 1
year, or both.
(2) PRIVATE APPLICATOR.—Any private applicator or other
person not included in paragraph (1) who knowingly violates
any provision of this Act shall be guilty of a misdemeanor and
shall on conviction be fined not more than $1,000, or imprisoned for not more than 30 days, or both.
(3) DISCLOSURE OF INFORMATION.—Any person, who, with
intent to defraud, uses or reveals information relative to formulas of products acquired under the authority of section 3,
shall be fined not more than $10,000, or imprisoned for not
more than three years, or both.
(4) ACTS OF OFFICERS, AGENTS, ETC.—When construing and
enforcing the provisions of this Act, the act, omission, or failure
of any officer, agent, or other person acting for or employed by
any person shall in every case be also deemed to be the act,
omission, or failure of such person as well as that of the person
employed.
SEC. 15. ø7 U.S.C. 136m¿ INDEMNITIES.

(a) GENERAL INDEMNIFICATION.—
(1) IN GENERAL.—Except as otherwise provided in this section, if—

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(A) the Administrator notifies a registrant under section 6(c)(1) that the Administrator intends to suspend a
registration or that an emergency order of suspension of a
registration under section 6(c)(3) has been issued;
(B) the registration in question is suspended under
section 6(c), and thereafter is canceled under section 6(b),
6(d), or 6(f); and
(C) any person who owned any quantity of the pesticide immediately before the notice to the registrant
under subparagraph (A) suffered losses by reason of suspension or cancellation of the registration;
the Administrator shall make an indemnity payment to the
person.
(2) EXCEPTION.—Paragraph (1) shall not apply if the Administrator finds that the person—
(A) had knowledge of facts that, in themselves, would
have shown that the pesticide did not meet the requirements of section 3(c)(5) for registration; and
(B) continued thereafter to produce the pesticide without giving timely notice of such facts to the Administrator.
(3) REPORT.—If the Administrator takes an action under
paragraph (1) that requires the payment of indemnification,
the Administrator shall report to the Committee on Agriculture
of the House of Representatives, the Committee on Agriculture,
Nutrition, and Forestry of the Senate, and the Committees on
Appropriations of the House of Representatives and the Senate
on—
(A) the action taken that requires the payment of
indemnification;
(B) the reasons for taking the action;
(C) the estimated cost of the payment; and
(D) a request for the appropriation of funds for the
payment.
(4) APPROPRIATION.—The Administrator may not make a
payment of indemnification under paragraph (1) unless a specific line item appropriation of funds has been made in advance
for the payment.
(b) INDEMNIFICATION OF END USERS, DEALERS, AND DISTRIBUTORS.—
(1) END USERS.—If—
(A) the Administrator notifies a registrant under section 6(c)(1) that the Administrator intends to suspend a
registration or that an emergency order of suspension of a
registration under section 6(c)(3) has been issued;
(B) the registration in question is suspended under
section 6(c), and thereafter is canceled under section 6(b),
6(d), or 6(f); and
(C) any person who, immediately before the notice to
the registrant under subparagraph (A), owned any quantity of the pesticide for purposes of applying or using the
pesticide as an end user, rather than for purposes of distributing or selling it or further processing it for distribution or sale, suffered a loss by reason of the suspension or
cancellation of the pesticide;
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Sec. 15

the person shall be entitled to an indemnity payment under
this subsection for such quantity of the pesticide.
(2) DEALERS AND DISTRIBUTORS.—
(A) Any registrant, wholesaler, dealer, or other distributor (hereinafter in this paragraph referred to as a
‘‘seller’’) of a registered pesticide who distributes or sells
the pesticide directly to any person not described as an
end user in paragraph (1)(C) shall, with respect to any
quantity of the pesticide that such person cannot use or resell as a result of the suspension or cancellation of the pesticide, reimburse such person for the cost of first acquiring
the pesticide from the seller (other than the cost of transportation, if any), unless the seller provided to the person
at the time of distribution or sale a notice, in writing, that
the pesticide is not subject to reimbursement by the seller.
(B) If—
(i) the Administrator notifies a registrant under
section 6(c)(1) that the Administrator intends to suspend a registration or that an emergency order of suspension of a registration under section 6(c)(3) has been
issued;
(ii) the registration in question is suspended
under section 6(c), and thereafter is canceled under
section 6(b), 6(d), or 6(f);
(iii) any person who, immediately before the notice
to the registrant under clause (i)—
(I) had not been notified in writing by the
seller, as provided under subparagraph (A), that
any quantity of the pesticide owned by such person is not subject to reimbursement by the seller
in the event of suspension or cancellation of the
pesticide; and
(II) owned any quantity of the pesticide for
purposes of—
(aa) distributing or selling it; or
(bb) further processing it for distribution
or sale directly to an end user;
suffered a loss by reason of the suspension or cancellation of the pesticide; and
(iv) the Administrator determines on the basis of
a claim of loss submitted to the Administrator by the
person, that the seller—
(I) did not provide the notice specified in subparagraph (A) to such person; and
(II) is and will continue to be unable to provide reimbursement to such person, as provided
under subparagraph (A), for the loss referred to in
clause (iii), as a result of the insolvency or bankruptcy of the seller and the seller’s resulting inability to provide such reimbursement;
the person shall be entitled to an indemnity payment
under this subsection for such quantity of the pesticide.
(C) If an indemnity payment is made by the United
States under this paragraph, the United States shall be
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subrogated to any right that would otherwise be held
under this paragraph by a seller who is unable to make a
reimbursement in accordance with this paragraph with regard to reimbursements that otherwise would have been
made by the seller.
(3) SOURCE.—Any payment required to be made under
paragraph (1) or (2) shall be made from the appropriation provided under section 1304 of title 31, United States Code.
(4) ADMINISTRATIVE SETTLEMENT.—An administrative settlement of a claim for such indemnity may be made in accordance with the third paragraph of section 2414 of title 28,
United States Code, and shall be regarded as if it were made
under that section for purposes of section 1304 of title 31,
United States Code.
(c) AMOUNT OF PAYMENT.—
(1) IN GENERAL.—The amount of an indemnity payment
under subsection (a) or (b) to any person shall be determined
on the basis of the cost of the pesticide owned by the person
(other than the cost of transportation, if any) immediately before the issuance of the notice to the registrant referred to in
subsection (a)(1)(A), (b)(1)(A), or (b)(2)(B)(i), except that in no
event shall an indemnity payment to any person exceed the
fair market value of the pesticide owned by the person immediately before the issuance of the notice.
(2) SPECIAL RULE.—Notwithstanding any other provision of
this Act, the Administrator may provide a reasonable time for
use or other disposal of the pesticide. In determining the quantity of any pesticide for which indemnity shall be paid under
this section, proper adjustment shall be made for any pesticide
used or otherwise disposed of by the owner.
SEC. 16. ø7 U.S.C. 136n¿ ADMINISTRATIVE PROCEDURE; JUDICIAL REVIEW.

(a) DISTRICT COURT REVIEW.—Except as otherwise provided in
this Act, the refusal of the Administrator to cancel or suspend a
registration or to change a classification not following a hearing
and other final actions of the Administrator not committed to the
discretion of the Administrator by law are judicially reviewable by
the district courts of the United States.
(b) REVIEW BY COURT OF APPEALS.—In the case of actual controversy as to the validity of any order issued by the Administrator
following a public hearing, any person who will be adversely affected by such order and who had been a party to the proceedings
may obtain judicial review by filing in the United States court of
appeals for the circuit wherein such person resides or has a place
of business, within 60 days after the entry of such order, a petition
praying that the order be set aside in whole or in part. A copy of
the petition shall be forthwith transmitted by the clerk of the court
to the Administrator or any officer designated by the Administrator
for that purpose, and thereupon the Administrator shall file in the
court the record of the proceedings on which the Administrator
based the Administrator’s order, as provided in section 2112 of title
28, United States Code. Upon the filing of such petition the court
shall have exclusive jurisdiction to affirm or set aside the order
complained of in whole or in part. The court shall consider all eviSeptember 28, 2012

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Sec. 17

dence of record. The order of the Administrator shall be sustained
if it is supported by substantial evidence when considered on the
record as a whole. The judgment of the court affirming or setting
aside, in whole or in part, any order under this section shall be
final, subject to review by the Supreme Court of the United States
upon certiorari or certification as provided in section 1254 of title
28 of the United States Code. The commencement of proceedings
under this section shall not, unless specifically ordered by the court
to the contrary, operate as a stay of an order.
(c) JURISDICTION OF DISTRICT COURTS.—The district courts of
the United States are vested with jurisdiction specifically to enforce, and to prevent and restrain violations of, this Act.
(d) NOTICE OF JUDGMENTS.—The Administrator shall, by publication in such manner as the Administrator may prescribe, give notice of all judgments entered in actions instituted under the authority of this Act.
SEC. 17. ø7 U.S.C. 136o¿ IMPORTS AND EXPORTS.

(a) PESTICIDES AND DEVICES INTENDED FOR EXPORT.—Notwithstanding any other provision this Act, no pesticide or device or active ingredient used in producing a pesticide intended solely for export to any foreign country shall be deemed in violation of this
Act—
(1) when prepared or packed according to the specifications
or directions of the foreign purchaser, except that producers of
such pesticides and devices and active ingredients used in producing pesticides shall be subject to sections 2(p), 2(q) (1) (A),
(C), (D), (E), (G), and (H), 2(q) (2) (A), (B), (C) (i) and (iii), and
(D), 7, and 8 of this Act; and
(2) in the case of any pesticide other than a pesticide registered under section 3 or sold under section 6(a) (1) of this
Act, if, prior to export, the foreign purchaser has signed a
statement acknowledging that the purchaser understands that
such pesticide is not registered for use in the United States
and cannot be sold in the United States under this Act.
A copy of that statement shall be transmitted to an appropriate official of the government of the importing country.
(b) CANCELLATION NOTICES FURNISHED TO FOREIGN GOVERNMENTS.—Whenever a registration, or a cancellation or suspension
of the registration of a pesticide becomes effective, or ceases to be
effective, the Administrator shall transmit through the State Department notification thereof to the governments of other countries
and to appropriate international agencies. Such notification shall,
upon request, include all information related to the cancellation or
suspension of the registration of the pesticide and information concerning other pesticides that are registered under section 3 of this
Act and that could be used in lieu of such pesticide.
(c) IMPORTATION OF PESTICIDES AND DEVICES.—The Secretary
of the Treasury shall notify the Administrator of the arrival of pesticides and devices and shall deliver to the Administrator, upon the
Administrator’s request, samples of pesticides or devices which are
being imported into the United States, giving notice to the owner
or consignee, who may appear before the Administrator and have
the right to introduce testimony. If it appears from the examination
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of a sample that it is adulterated, or misbranded or otherwise violates the provisions set forth in this Act, or is otherwise injurious
to health or the environment, the pesticide or device may be refused admission, and the Secretary of the Treasury shall refuse delivery to the consignee and shall cause the destruction of any pesticide or device refused delivery which shall not be exported by the
consignee within 90 days from the date of notice of such refusal
under such regulations as the Secretary of the Treasury may prescribe. The Secretary of the Treasury may deliver to the consignee
such pesticide or device pending examination and decision in the
matter on execution of bond for the amount of the full invoice value
of such pesticide or device, together with the duty thereon, and on
refusal to return such pesticide or device for any cause to the custody of the Secretary of the Treasury, when demanded, for the purpose of excluding them from the country, or for any other purpose,
said consignee shall forfeit the full amount of said bond. All
charges for storage, cartage, and labor on pesticides or devices
which are refused admission or delivery shall be paid by the owner
or consignee, and in default of such payment shall constitute a lien
against any future importation made by such owner or consignee.
(d) COOPERATION IN INTERNATIONAL EFFORTS.—
(1) IN GENERAL.—The Administrator shall, in cooperation
with the Department of State and any other appropriate Federal agency, participate and cooperate in any international efforts to develop improved pesticide research and regulations.
(2) DEPARTMENT OF STATE EXPENSES.—Any expenses incurred by an employee of the Environmental Protection Agency
who participates in any international technical, economic, or
policy review board, committee, or other official body that is
meeting in relation to an international treaty shall be paid by
the Department of State.
(e) REGULATIONS.—The Secretary of the Treasury, in consultation with the Administrator, shall prescribe regulations for the enforcement of subsection (c) of this section.
SEC. 18. ø7 U.S.C. 136p¿ EXEMPTION OF FEDERAL AND STATE AGENCIES.

The Administrator may, at the Administrator’s discretion, exempt any Federal or State agency from any provision of this Act
if the Administrator determines that emergency conditions exist
which require such exemption. The Administrator, in determining
whether or not such emergency conditions exist, shall consult with
the Secretary of Agriculture and the Governor of any State concerned if they request such determination.
SEC. 19. ø7 U.S.C. 136q¿ STORAGE, DISPOSAL, TRANSPORTATION, AND
RECALL.

(a) STORAGE, DISPOSAL, AND TRANSPORTATION.—
(1) DATA REQUIREMENTS AND REGISTRATION OF PESTICIDES.—The Administrator may require under section 3 or 6
that—
(A) the registrant or applicant for registration of a pesticide submit or cite data or information regarding methods for the safe storage and disposal of excess quantities

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Sec. 19

of the pesticide to support the registration or continued
registration of a pesticide;
(B) the labeling of a pesticide contain requirements
and procedures for the transportation, storage, and disposal of the pesticide, any container of the pesticide, any
rinsate containing the pesticide, or any other material
used to contain or collect excess or spilled quantities of the
pesticide; and
(C) the registrant of a pesticide provide evidence of
sufficient financial and other resources to carry out a recall plan under subsection (b), and provide for the disposition of the pesticide, in the event of suspension and cancellation of the pesticide.
(2) PESTICIDES.—The Administrator may by regulation, or
as part of an order issued under section 6 or an amendment
to such an order—
(A) issue requirements and procedures to be followed
by any person who stores or transports a pesticide the registration of which has been suspended or canceled;
(B) issue requirements and procedures to be followed
by any person who disposes of stocks of a pesticide the registration of which has been suspended; and
(C) issue requirements and procedures for the disposal
of any pesticide the registration of which has been canceled.
(3) CONTAINERS, RINSATES, AND OTHER MATERIALS.—The
Administrator may by regulation, or as part of an order issued
under section 6 or an amendment to such an order—
(A) issue requirements and procedures to be followed
by any person who stores or transports any container of a
pesticide the registration of which has been suspended or
canceled, any rinsate containing the pesticide, or any other
material used to contain or collect excess or spilled quantities of the pesticide;
(B) issue requirements and procedures to be followed
by any person who disposes of stocks of any container of
a pesticide the registration of which has been suspended,
any rinsate containing the pesticide, or any other material
used to contain or collect excess or spilled quantities of the
pesticide; and
(C) issue requirements and procedures for the disposal
of any container of a pesticide the registration of which
has been canceled, any rinsate containing the pesticide, or
any other material used to contain or collect excess or
spilled quantities of the pesticide.
(4) CONTAINER RECYCLING.—The Secretary may promulgate a regulation for the return and recycling of disposable pesticide containers used for the distribution or sale of registered
pesticide products in interstate commerce. Any such regulation
requiring recycling of disposable pesticide containers shall not
apply to antimicrobial pesticides (as defined in section 2) or
other pesticide products intended for non-agricultural uses.
(b) RECALLS.—
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(1) IN GENERAL.—If the registration of a pesticide has been
suspended and canceled under section 6, and if the Administrator finds that recall of the pesticide is necessary to protect
health or the environment, the Administrator shall order a recall of the pesticide in accordance with this subsection.
(2) VOLUNTARY RECALL.—If, after determining under paragraph (1) that a recall is necessary, the Administrator finds
that voluntary recall by the registrant and others in the chain
of distribution may be as safe and effective as a mandatory recall, the Administrator shall request the registrant of the pesticide to submit, within 60 days of the request, a plan for the
voluntary recall of the pesticide. If such a plan is requested
and submitted, the Administrator shall approve the plan and
order the registrant to conduct the recall in accordance with
the plan unless the Administrator determines, after an informal hearing, that the plan is inadequate to protect health or
the environment.
(3) MANDATORY RECALL.—If, after determining under paragraph (1) that a recall is necessary, the Administrator does not
request the submission of a plan under paragraph (2) or finds
such a plan to be inadequate, the Administrator shall issue a
regulation that prescribes a plan for the recall of the pesticide.
A regulation issued under this paragraph may apply to any
person who is or was a registrant, distributor, or seller of the
pesticide, or any successor in interest to such a person.
(4) RECALL PROCEDURE.—A regulation issued under this
subsection may require any person that is subject to the regulation to—
(A) arrange to make available one or more storage facilities to receive and store the pesticide to which the recall program applies, and inform the Administrator of the
location of each such facility;
(B) accept and store at such a facility those existing
stocks of such pesticide that are tendered by any other
person who obtained the pesticide directly or indirectly
from the person that is subject to such regulation;
(C) on the request of a person making such a tender,
provide for proper transportation of the pesticide to a storage facility; and
(D) take such reasonable steps as the regulation may
prescribe to inform persons who may be holders of the pesticide of the terms of the recall regulation and how those
persons may tender the pesticide and arrange for transportation of the pesticide to a storage facility.
(5) CONTENTS OF RECALL PLAN.—A recall plan established
under this subsection shall include—
(A) the level in the distribution chain to which the recall is to extend, and a schedule for recall; and
(B) the means to be used to verify the effectiveness of
the recall.
(6) REQUIREMENTS OR PROCEDURES.—No requirement or
procedure imposed in accordance with paragraph (2) of subsection (a) may require the recall of existing stocks of the pesticide except as provided by this subsection.
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(c) STORAGE COSTS.—
(1) SUBMISSION OF PLAN.—A registrant who wishes to become eligible for reimbursement of storage costs incurred as a
result of a recall prescribed under subsection (b) for a pesticide
whose registration has been suspended and canceled shall, as
soon as practicable after the suspension of the registration of
the pesticide, submit to the Administrator a plan for the storage and disposal of the pesticide that meets criteria established
by the Administrator by regulation.
(2) REIMBURSEMENT.—Within a reasonable period of time
after such storage costs are incurred and paid by the registrant, the Administrator shall reimburse the registrant, on
request, for—
(A) none of the costs incurred by the registrant before
the date of submission of the plan referred to in paragraph
(1) to the Administrator;
(B) 100 percent of the costs incurred by the registrant
after the date of submission of the plan to the Administrator or the date of cancellation of the registration of the
pesticide, whichever is later, but before the approval of the
plan by the Administrator;
(C) 50 percent of the costs incurred by the registrant
during the 1-year period beginning on the date of the approval of the plan by the Administrator or the date of cancellation of the registration of the pesticide, whichever is
later;
(D) none of the costs incurred by the registrant during
the 3-year period beginning on the 366th day following approval of the plan by the Administrator or the date of cancellation of the registration of the pesticide, whichever is
later; and
(E) 25 percent of the costs incurred by the registrant
during the period beginning on the first day of the 5th
year following the date of the approval of the plan by the
Administrator or the date of cancellation of the registration of the pesticide, whichever is later, and ending on the
date that a disposal permit for the pesticide is issued by
a State or an alternative plan for disposal of the pesticide
in accordance with applicable law has been developed.
(d) ADMINISTRATION OF STORAGE, DISPOSAL, TRANSPORTATION,
AND RECALL PROGRAMS.—
(1) VOLUNTARY AGREEMENTS.—Nothing in this section
shall be construed as preventing or making unlawful any
agreement between a seller and a buyer of any pesticide or
other substance regarding the ultimate allocation of the costs
of storage, transportation, or disposal of a pesticide.
(2) RULE AND REGULATION REVIEW.—Section 25(a)(4) shall
not apply to any regulation issued under subsection (a)(2) or
(b).
(3) LIMITATIONS.—No registrant shall be responsible under
this section for a pesticide the registration of which is held by
another person. No distributor or seller shall be responsible
under this section for a pesticide that the distributor or seller
did not hold or sell.
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(4) SEIZURE AND PENALTIES.—If the Administrator finds
that a person who is subject to a regulation or order under
subsection (a)(2) or (b) has failed substantially to comply with
that regulation or order, the Administrator may take action
under section 13 or 14 or obtain injunctive relief under section
16(c) against such person or any successor in interest of any
such person.
(e) CONTAINER DESIGN.—
(1) PROCEDURES.—
(A) Not later than 3 years after the effective date of
this subsection [December 24, 1988], the Administrator
shall, in consultation with the heads of other interested
Federal agencies, promulgate regulations for the design of
pesticide containers that will promote the safe storage and
disposal of pesticides.
(B) The regulations shall ensure, to the fullest extent
practicable, that the containers—
(i) accommodate procedures used for the removal
of pesticides from the containers and the rinsing of the
containers;
(ii) facilitate the safe use of the containers, including elimination of splash and leakage of pesticides
from the containers;
(iii) facilitate the safe disposal of the containers;
and
(iv) facilitate the safe refill and reuse of the
containers.
(2) COMPLIANCE.—The Administrator shall require compliance with the regulations referred to in paragraph (1) not later
than 5 years after the effective date of this subsection [December 24, 1988].
(f) PESTICIDE RESIDUE REMOVAL.—
(1) PROCEDURES.—
(A) Not later than 3 years after the effective date of
this subsection [December 24, 1988], the Administrator
shall, in consultation with the heads of other interested
Federal agencies, promulgate regulations prescribing procedures and standards for the removal of pesticides from
containers prior to disposal.
(B) The regulations may—
(i) specify, for each major type of pesticide container, procedures and standards providing for, at a
minimum, triple rinsing or the equivalent degree of
pesticide removal;
(ii) specify procedures that can be implemented
promptly and easily in various circumstances and conditions;
(iii) provide for reuse, whenever practicable, or
disposal of rinse water and residue; and
(iv) be coordinated with requirements for the rinsing of containers imposed under the Solid Waste Disposal Act (42 U.S.C. 6901 et seq.).
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(C) The Administrator may, at the discretion of the
Administrator, exempt products intended solely for household use from the requirements of this subsection.
(2) COMPLIANCE.—Effective beginning 5 years after the effective date of this subsection [December 24, 1988], a State
may not exercise primary enforcement responsibility under section 26, or certify an applicator under section 11, unless the
Administrator determines that the State is carrying out an
adequate program to ensure compliance with this subsection.
(3) SOLID WASTE DISPOSAL ACT.—Nothing in this subsection
shall affect the authorities or requirements concerning pesticide containers under the Solid Waste Disposal Act (42 U.S.C.
6901).
(g) PESTICIDE CONTAINER STUDY.—
(1) STUDY.—
(A) The Administrator shall conduct a study of options
to encourage or require—
(i) the return, refill, and reuse of pesticide containers;
(ii) the development and use of pesticide formulations that facilitate the removal of pesticide residues
from containers; and
(iii) the use of bulk storage facilities to reduce the
number of pesticide containers requiring disposal.
(B) In conducting the study, the Administrator shall—
(i) consult with the heads of other interested Federal agencies, State agencies, industry groups, and environmental organizations; and
(ii) assess the feasibility, costs, and environmental
benefits of encouraging or requiring various measures
or actions.
(2) REPORT.—Not later than 2 years after the effective date
of this subsection [December 24, 1988], the Administrator shall
submit to Congress a report describing the results of the study
required under paragraph (1).
(h) RELATIONSHIP TO SOLID WASTE DISPOSAL ACT.—
(1) IN GENERAL.—Nothing in this section shall diminish
the authorities or requirements of the Solid Waste Disposal Act
(42 U.S.C. 6901 et seq.).
(2) ANTIMICROBIAL PRODUCTS.—A household, industrial, or
institutional antimicrobial product that is not subject to regulation under the Solid Waste Disposal Act (42 U.S.C. 6901 et
seq.) shall not be subject to the provisions of subsections (a),
(e), and (f), unless the Administrator determines that such
product must be subject to such provisions to prevent an unreasonable adverse effect on the environment.
SEC. 20. ø7 U.S.C. 136r¿ RESEARCH AND MONITORING.

(a) RESEARCH.—The Administrator shall undertake research,
including research by grant or contract with other Federal agencies, universities, or others as may be necessary to carry out the
purposes of this Act, and the Administrator shall conduct research
into integrated pest management in coordination with the Secretary of Agriculture. The Administrator shall also take care to enSeptember 28, 2012

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sure that such research does not duplicate research being undertaken by any other Federal agency.
(b) NATIONAL MONITORING PLAN.—The Administrator shall formulate and periodically revise, in cooperation with other Federal,
State, or local agencies, a national plan for monitoring pesticides.
(c) MONITORING.—The Administrator shall undertake such
monitoring activities, including, but not limited to monitoring in
air, soil, water, man, plants, and animals, as may be necessary for
the implementation of this Act and of the national pesticide monitoring plan. The Administrator shall establish procedures for the
monitoring of man and animals and their environment for incidental pesticide exposure, including, but not limited to, the quantification of incidental human and environmental pesticide pollution and the secular trends thereof, and identification of the
sources of contamination and their relationship to human and environmental effects. Such activities shall be carried out in cooperation with other Federal, State, and local agencies.
SEC. 21. ø7 U.S.C. 136s¿ SOLICITATION OF COMMENTS; NOTICE OF PUBLIC HEARINGS.

(a) SECRETARY OF AGRICULTURE.—The Administrator, before
publishing regulations under this Act, shall solicit the views of the
Secretary of Agriculture in accordance with the procedure described
in section 25(a).
(b) SECRETARY OF HEALTH AND HUMAN SERVICES.—The Administrator, before publishing regulations under this Act for any public
health pesticide, shall solicit the views of the Secretary of Health
and Human Services in the same manner as the views of the Secretary of Agriculture are solicited under section 25(a)(2).
(c) VIEWS.—In addition to any other authority relating to public hearings and solicitation of views, in connection with the suspension or cancellation of a pesticide registration or any other actions authorized under this Act, the Administrator may, at the Administrator’s discretion, solicit the views of all interested persons,
either orally or in writing, and seek such advice from scientists,
farmers, farm organizations, and other qualified persons as the Administrator deems proper.
(d) NOTICE.—In connection with all public hearings under this
Act the Administrator shall publish timely notice of such hearings
in the Federal Register.
SEC. 22. ø7 U.S.C. 136t¿ DELEGATION AND COOPERATION.

(a) DELEGATION.—All authority vested in the Administrator by
virtue of the provisions of this Act may with like force and effect
be executed by such employees of the Environmental Protection
Agency as the Administrator may designate for the purpose.
(b) COOPERATION.—The Administrator shall cooperate with the
Department of Agriculture, any other Federal agency, and any appropriate agency of any State or any political subdivision thereof,
in carrying out the provisions of this Act, and in securing uniformity of regulations.
SEC. 23. ø7 U.S.C. 136u¿ STATE COOPERATION, AID, AND TRAINING.

(a) COOPERATIVE AGREEMENTS.—The Administrator may enter
into cooperative agreements with States and Indian tribes—
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(1) to delegate to any State or Indian tribe the authority
to cooperate in the enforcement of this Act through the use of
its personnel or facilities, to train personnel of the State or Indian tribe to cooperate in the enforcement of this Act, and to
assist States and Indian tribes in implementing cooperative enforcement programs through grants-in-aid; and
(2) to assist States in developing and administering State
programs, and Indian tribes that enter into cooperative agreements, to train and certify applicators consistent with the
standards the Administrator prescribes.
Effective with the fiscal year beginning October 1, 1978, there are
authorized to be appropriated annually such funds as may be necessary for the Administrator to provide through cooperative agreements an amount equal to 50 percent of the anticipated cost to
each State or Indian tribe, as agreed to under such cooperative
agreements, of conducting training and certification programs during such fiscal year. If funds sufficient to pay 50 percent of the
costs for any year are not appropriated, the share of each State and
Indian tribe shall be reduced in a like proportion in allocating
available funds.
(b) CONTRACTS FOR TRAINING.—In addition, the Administrator
may enter into contracts with Federal, State, or Indian tribal agencies for the purpose of encouraging the training of certified applicators.
(c) INFORMATION AND EDUCATION.—The Administrator shall, in
cooperation with the Secretary of Agriculture, use the services of
the cooperative State extension services to inform and educate pesticide users about accepted uses and other regulations made under
this Act.
SEC. 24. ø7 U.S.C. 136v¿ AUTHORITY OF STATES.

(a) IN GENERAL.—A State may regulate the sale or use of any
federally registered pesticide or device in the State, but only if and
to the extent the regulation does not permit any sale or use prohibited by this Act.
(b) UNIFORMITY.—Such State shall not impose or continue in
effect any requirements for labeling or packaging in addition to or
different from those required under this Act.
(c) ADDITIONAL USES.—
(1) A State may provide registration for additional uses of
federally registered pesticides formulated for distribution and
use within that State to meet special local needs in accord with
the purposes of this Act and if registration for such use has not
previously been denied, disapproved, or canceled by the Administrator. Such registration shall be deemed registration under
section 3 for all purposes of this Act, but shall authorize distribution and use only within such State.
(2) A registration issued by a State under this subsection
shall not be effective for more than ninety days if disapproved
by the Administrator within that period. Prior to disapproval,
the Administrator shall, except as provided in paragraph (3) of
this subsection, advise the State of the Administrator’s intention to disapprove and the reasons therefor, and provide the
State time to respond. The Administrator shall not prohibit or
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disapprove a registration issued by a State under this subsection (A) on the basis of lack of essentiality of a pesticide or
(B) except as provided in paragraph (3) of this subsection, if its
composition and use patterns are similar to those of a federally
registered pesticide.
(3) In no instance may a State issue a registration for a
food or feed use unless there exists a tolerance or exemption
under the Federal Food, Drug, and Cosmetic Act that permits
the residues of the pesticide on the food or feed. If the Administrator determines that a registration issued by a State is inconsistent with the Federal Food, Drug, and Cosmetic Act, or
the use of, a pesticide under a registration issued by a State
constitutes an imminent hazard, the Administrator may immediately disapprove the registration.
(4) If the Administrator finds, in accordance with standards set forth in regulations issued under section 25 of this
Act, that a State is not capable of exercising adequate controls
to assure that State registration under this section will be in
accord with the purposes of this Act or has failed to exercise
adequate controls, the Administrator may suspend the authority of the State to register pesticides until such time as the Administrator is satisfied that the State can and will exercise
adequate controls. Prior to any such suspension, the Administrator shall advise the State of the Administrator’s intention to
suspend and the reasons therefor and provide the State time
to respond.
SEC. 25. ø7 U.S.C. 136w¿ AUTHORITY OF ADMINISTRATOR.

(a) IN GENERAL.—
(1) REGULATIONS.—The Administrator is authorized in accordance with the procedure described in paragraph (2), to prescribe regulations to carry out the provisions of this Act. Such
regulations shall take into account the difference in concept
and usage between various classes of pesticides, including public health pesticides, and differences in environmental risk and
the appropriate data for evaluating such risk between agricultural, nonagricultural, and public health pesticides.
(2) PROCEDURE.—
(A) PROPOSED REGULATIONS.—At least 60 days prior to
signing any proposed regulation for publication in the Federal Register, the Administrator shall provide the Secretary of Agriculture with a copy of such regulation. If the
Secretary comments in writing to the Administrator regarding any such regulation within 30 days after receiving
it, the Administrator shall publish in the Federal Register
(with the proposed regulation) the comments of the Secretary and the response of the Administrator with regard
to the Secretary’s comments. If the Secretary does not
comment in writing to the Administrator regarding the
regulation within 30 days after receiving it, the Administrator may sign such regulation for publication in the Federal Register any time after such 30-day period notwithstanding the foregoing 60-day time requirement.

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(B) FINAL REGULATIONS.—At least 30 days prior to
signing any regulation in final form for publication in the
Federal Register, the Administrator shall provide the Secretary of Agriculture with a copy of such regulation. If the
Secretary comments in writing to the Administrator regarding any such final regulation within 15 days after receiving it, the Administrator shall publish in the Federal
Register (with the final regulation) the comments of the
Secretary, if requested by the Secretary, and the response
of the Administrator concerning the Secretary’s comments.
If the Secretary does not comment in writing to the Administrator regarding the regulation within 15 days after
receiving it, the Administrator may sign such regulation
for publication in the Federal Register at any time after
such 15-day period notwithstanding the foregoing 30-day
time requirement. In taking any final action under this
subsection, the Administrator shall include among those
factors to be taken into account the effect of the regulation
on production and prices of agricultural commodities, retail food prices, and otherwise on the agricultural economy,
and the Administrator shall publish in the Federal Register an analysis of such effect.
(C) TIME REQUIREMENTS.—The time requirements imposed by subparagraphs (A) and (B) may be waived or
modified to the extent agreed upon by the Administrator
and the Secretary.
(D) PUBLICATION IN THE FEDERAL REGISTER.—The Administrator shall, simultaneously with any notification to
the Secretary of Agriculture under this paragraph prior to
the issuance of any proposed or final regulation, publish
such notification in the Federal Register.
(3) CONGRESSIONAL COMMITTEES.—At such time as the Administrator is required under paragraph (2) of this subsection
to provide the Secretary of Agriculture with a copy of proposed
regulations and a copy of the final form of regulations, the Administrator shall also furnish a copy of such regulations to the
Committee on Agriculture of the House of Representatives and
the Committee on Agriculture, Nutrition, and Forestry of the
Senate.
(4) CONGRESSIONAL REVIEW OF REGULATIONS.—Simultaneously with the promulgation of any rule or regulation under
this Act, the Administrator shall transmit a copy thereof to the
Secretary of the Senate and the Clerk of the House of Representatives. The rule or regulation shall not become effective
until the passage of 60 calendar days after the rule or regulation is so transmitted.
(b) EXEMPTION OF PESTICIDES.—The Administrator may exempt from the requirements of this Act by regulation any pesticide
which the Administrator determines either (1) to be adequately
regulated by another Federal agency, or (2) to be of a character
which is unnecessary to be subject to this Act in order to carry out
the purposes of this Act.
(c) OTHER AUTHORITY.—The Administrator, after notice and
opportunity for hearing, is authorized—
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(1) to declare a pest any form of plant or animal life (other
than man and other than bacteria, virus, and other micro-organisms on or in living man or other living animals) which is injurious to health or the environment;
(2) to determine any pesticide which contains any substance or substances in quantities highly toxic to man;
(3) to establish standards (which shall be consistent with
those established under the authority of the Poison Prevention
Packaging Act (Public Law 91–601)) with respect to the package, container, or wrapping in which a pesticide or device is
enclosed for use or consumption, in order to protect children
and adults from serious injury or illness resulting from accidental ingestion or contact with pesticides or devices regulated
by this Act as well as to accomplish the other purposes of this
Act;
(4) to specify those classes of devices which shall be subject
to any provision of paragraph 2(q)(1) or section 7 of this Act
upon the Administrator’s determination that application of
such provision is necessary to effectuate the purposes of this
Act;
(5) to prescribe regulations requiring any pesticide to be
colored or discolored if the Administrator determines that such
requirement is feasible and is necessary for the protection of
health and the environment; and
(6) to determine and establish suitable names to be used
in the ingredient statement.
(d) SCIENTIFIC ADVISORY PANEL.—
(1) IN GENERAL.—The Administrator shall submit to an advisory panel for comment as to the impact on health and the
environment of the action proposed in notices of intent issued
under section 6(b) and of the proposed and final form of regulations issued under section 25(a) within the same time periods
as provided for the comments of the Secretary of Agriculture
under such sections. The time requirements for notices of intent and proposed and final forms of regulation may not be
modified or waived unless in addition to meeting the requirements of section 6(b) or 25(a), as applicable, the advisory panel
has failed to comment on the proposed action within the prescribed time period or has agreed to the modification or waiver.
The Administrator shall also solicit from the advisory panel
comments, evaluations, and recommendations for operating
guidelines to improve the effectiveness and quality of scientific
analyses made by personnel of the Environmental Protection
Agency that lead to decisions by the Administrator in carrying
out the provisions of this Act. The comments, evaluations, and
recommendations of the advisory panel submitted under this
subsection and the response of the Administrator shall be published in the Federal Register in the same manner as provided
for publication of the comments of the Secretary of Agriculture
under such sections. The chairman of the advisory panel, after
consultation with the Administrator, may create temporary
subpanels on specific projects to assist the full advisory panel
in expediting and preparing its evaluations, comments, and
recommendations. The subpanels may be composed of sciSeptember 28, 2012

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entists other than members of the advisory panel, as deemed
necessary for the purpose of evaluating scientific studies relied
upon by the Administrator with respect to proposed action.
Such additional scientists shall be selected by the advisory
panel. The panel referred to in this subsection shall consist of
7 members appointed by the Administrator from a list of 12
nominees, 6 nominated by the National Institutes of Health
and 6 by the National Science Foundation, utilizing a system
of staggered terms of appointment. Members of the panel shall
be selected on the basis of their professional qualifications to
assess the effects of the impact of pesticides on health and the
environment. To the extent feasible to insure multidisciplinary
representation, the panel membership shall include representation from the disciplines of toxicology, pathology, environmental biology, and related sciences. If a vacancy occurs on the
panel due to expiration of a term, resignation, or any other
reason, each replacement shall be selected by the Administrator from a group of 4 nominees, 2 submitted by each of the
nominating entities named in this subsection. The Administrator may extend the term of a panel member until the new
member is appointed to fill the vacancy. If a vacancy occurs
due to resignation, or reason other than expiration of a term,
the Administrator shall appoint a member to serve during the
unexpired term utilizing the nomination process set forth in
this subsection. Should the list of nominees provided under
this subsection be unsatisfactory, the Administrator may request an additional set of nominees from the nominating entities. The Administrator may require such information from the
nominees to the advisory panel as the Administrator deems
necessary, and the Administrator shall publish in the Federal
Register the name, address, and professional affiliations of
each nominee. Each member of the panel shall receive per
diem compensation at a rate not in excess of that fixed for GS–
18 of the General Schedule as may be determined by the Administrator, except that any such member who holds another
office or position under the Federal Government the compensation for which exceeds such rate may elect to receive compensation at the rate provided for such other office or position
in lieu of the compensation provided by this subsection. In
order to assure the objectivity of the advisory panel, the Administrator shall promulgate regulations regarding conflicts of
interest with respect to the members of the panel. The advisory panel established under this section shall be permanent.
In performing the functions assigned by this Act, the panel
shall consult and coordinate its activities with the Science Advisory Board established under the Environmental Research,
Development, and Demonstration Authorization Act of 1978.
Whenever the Administrator exercises authority under section
6(c) of this Act to immediately suspend the registration of any
pesticide to prevent an imminent hazard, the Administrator
shall promptly submit to the advisory panel for comment, as
to the impact on health and the environment, the action taken
to suspend the registration of such pesticide.
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(2) SCIENCE REVIEW BOARD.—There is established a
Science Review Board to consist of 60 scientists who shall be
available to the Scientific Advisory Panel to assist in reviews
conducted by the Panel. Members of the Board shall be selected in the same manner as members of temporary subpanels
created under paragraph (1). Members of the Board shall be
compensated in the same manner as members of the Panel.
(e) PEER REVIEW.—The Administrator shall, by written procedures, provide for peer review with respect to the design, protocols,
and conduct of major scientific studies conducted under this Act by
the Environmental Protection Agency or by any other Federal
agency, any State or political subdivision thereof, or any institution
or individual under grant, contract, or cooperative agreement from
or with the Environmental Protection Agency. In such procedures,
the Administrator shall also provide for peer review, using the advisory panel established under subsection (d) of this section or appropriate experts appointed by the Administrator from a current
list of nominees maintained by such panel, with respect to the results of any such scientific studies relied upon by the Administrator
with respect to actions the Administrator may take relating to the
change in classification, suspension, or cancellation of a pesticide.
Whenever the Administrator determines that circumstances do not
permit the peer review of the results of any such scientific study
prior to the Administrator’s exercising authority under section 6(c)
of this Act to immediately suspend the registration of any pesticide
to prevent an imminent hazard, the Administrator shall promptly
thereafter provide for the conduct of peer review as provided in this
sentence. The evaluations and relevant documentation constituting
the peer review that relate to the proposed scientific studies and
the results of the completed scientific studies shall be included in
the submission for comment forwarded by the Administrator to the
advisory panel as provided in subsection (d). As used in this subsection, the term ‘‘peer review’’ shall mean an independent evaluation by scientific experts, either within or outside the Environmental Protection Agency, in the appropriate disciplines.
SEC. 26. ø7 U.S.C. 136w–1¿ STATE PRIMARY ENFORCEMENT RESPONSIBILITY.

(a) IN GENERAL.—For the purposes of this Act, a State shall
have primary enforcement responsibility for pesticide use violations
during any period for which the Administrator determines that
such State—
(1) has adopted adequate pesticide use laws and regulations, except that the Administrator may not require a State
to have pesticide use laws that are more stringent than this
Act;
(2) has adopted and is implementing adequate procedures
for the enforcement of such State laws and regulations; and
(3) will keep such records and make such reports showing
compliance with paragraphs (1) and (2) of this subsection as
the Administrator may require by regulation.
(b) SPECIAL RULES.—Notwithstanding the provisions of subsection (a) of this section, any State that enters into a cooperative
agreement with the Administrator under section 23 of this Act for
the enforcement of pesticide use restrictions shall have the primary
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enforcement responsibility for pesticide use violations. Any State
that has a plan approved by the Administrator in accordance with
the requirements of section 11 of this Act that the Administrator
determines meets the criteria set out in subsection (a) of this section shall have the primary enforcement responsibility for pesticide
use violations. The Administrator shall make such determinations
with respect to State plans under section 11 of this Act in effect
on the date of enactment of the Federal Pesticide Act of 1978 [September 30, 1978] not later than six months after that date.
(c) ADMINISTRATOR.—The Administrator shall have primary enforcement responsibility for those States that do not have primary
enforcement responsibility under this Act. Notwithstanding the
provisions of section 2(e)(1) of this Act, during any period when the
Administrator has such enforcement responsibility, section 8(b) of
this Act shall apply to the books and records of commercial applicators and to any applicator who holds or applies pesticides, or uses
dilutions of pesticides, only to provide a service of controlling pests
without delivering any unapplied pesticide to any person so served,
and section 9(a) of this Act shall apply to the establishment or
other place where pesticides or devices are held for application by
such persons with respect to pesticides or devices held for such application.
SEC. 27. ø7 U.S.C. 136w–2¿ FAILURE BY THE STATE TO ASSURE ENFORCEMENT OF STATE PESTICIDE USE REGULATIONS.

(a) REFERRAL.—Upon receipt of any complaint or other information alleging or indicating a significant violation of the pesticide
use provisions of this Act, the Administrator shall refer the matter
to the appropriate State officials for their investigation of the matter consistent with the requirements of this Act. If, within thirty
days, the State has not commenced appropriate enforcement action,
the Administrator may act upon the complaint or information to
the extent authorized under this Act.
(b) NOTICE.—Whenever the Administrator determines that a
State having primary enforcement responsibility for pesticide use
violations is not carrying out (or cannot carry out due to the lack
of adequate legal authority) such responsibility, the Administrator
shall notify the State. Such notice shall specify those aspects of the
administration of the State program that are determined to be inadequate. The State shall have ninety days after receipt of the notice to correct any deficiencies. If after that time the Administrator
determines that the State program remains inadequate, the Administrator may rescind, in whole or in part, the State’s primary
enforcement responsibility for pesticide use violations.
(c) CONSTRUCTION.—Neither section 26 of this Act nor this section shall limit the authority of the Administrator to enforce this
Act, where the Administrator determines that emergency conditions exist that require immediate action on the part of the Administrator and the State authority is unwilling or unable adequately
to respond to the emergency.
SEC. 28. ø7 U.S.C. 136w–3¿ IDENTIFICATION OF PESTS; COOPERATION
WITH DEPARTMENT OF AGRICULTURE’S PROGRAM.

(a) IN GENERAL.—The Administrator, in coordination with the
Secretary of Agriculture, shall identify those pests that must be
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brought under control. The Administrator shall also coordinate and
cooperate with the Secretary of Agriculture’s research and implementation programs to develop and improve the safe use and effectiveness of chemical, biological, and alternative methods to combat
and control pests that reduce the quality and economical production and distribution of agricultural products to domestic and foreign consumers.
(b) PEST CONTROL AVAILABILITY.—
(1) IN GENERAL.—The Administrator, in cooperation with
the Secretary of Agriculture, shall identify—
(A) available methods of pest control by crop or animal;
(B) minor pest control problems, both in minor crops
and minor or localized problems in major crops; and
(C) factors limiting the availability of specific pest control methods, such as resistance to control methods and
regulatory actions limiting the availability of control methods.
(2) REPORT.—The Secretary of Agriculture shall, not later
than 180 days after the date of enactment of this subsection
[November 28, 1990] and annually thereafter, prepare a report
and send the report to the Administrator. The report shall—
(A) contain the information described in paragraph (1)
and the information required by section 1651 of the Food,
Agriculture, Conservation, and Trade Act of 1990;
(B) identify the crucial pest control needs where a
shortage of control methods is indicated by the information
described in paragraph (1); and
(C) describe in detail research and extension efforts
designed to address the needs identified in subparagraph
(B).
(c) INTEGRATED PEST MANAGEMENT.—The Administrator, in
cooperation with the Secretary of Agriculture, shall develop
approaches to the control of pests based on integrated pest management that respond to the needs of producers, with a special emphasis on minor pests.
(d) PUBLIC HEALTH PESTS.—The Administrator, in coordination
with the Secretary of Agriculture and the Secretary of Health and
Human Services, shall identify pests of significant public health
importance and, in coordination with the Public Health Service, develop and implement programs to improve and facilitate the safe
and necessary use of chemical, biological, and other methods to
combat and control such pests of public health importance.
SEC. 29. ø7 U.S.C. 136w–4¿ ANNUAL REPORT.

The Administrator shall submit an annual report to Congress
before February 16 of each year and the first report shall be due
February 15, 1979. The report shall include the total number of applications for conditional registration under sections 3(c)(7)(B) and
3(c)(7)(C) of this Act that were filed during the immediately preceding fiscal year, and, with respect to those applications approved,
the Administrator shall report the Administrator’s findings in each
case, the conditions imposed and any modification of such conditions in each case, and the quantities produced of such pesticides.
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SEC. 30. ø7 U.S.C. 136w–5¿ MINIMUM REQUIREMENTS FOR TRAINING OF
MAINTENANCE APPLICATORS AND SERVICE TECHNICIANS.

Each State may establish minimum requirements for training
of maintenance applicators and service technicians. Such training
may include instruction in the safe and effective handling and use
of pesticides in accordance with the Environmental Protection
Agency approved labeling, and instruction in integrated pest management techniques. The authority of the Administrator with respect to minimum requirements for training of maintenance applicators and service technicians shall be limited to ensuring that
each State understands the provisions of this section.
SEC. 31. ø7 U.S.C. 136w–6¿ ENVIRONMENTAL PROTECTION AGENCY
MINOR USE PROGRAM.

(a) The Administrator shall assure coordination of minor use
issues through the establishment of a minor use program within
the Office of Pesticide Programs. Such office shall be responsible
for coordinating the development of minor use programs and policies and consulting with growers regarding minor use issues and
registrations and amendments which are submitted to the Environmental Protection Agency.
(b) The Office of Pesticide Programs shall prepare a public report concerning the progress made on the registration of minor
uses, including implementation of the exclusive use as an incentive
for registering new minor uses, within 3 years of the passage of the
Food Quality Protection Act of 1996. [Aug. 3, 1996]
SEC. 32. ø7 U.S.C. 136w–7¿ DEPARTMENT OF AGRICULTURE MINOR USE
PROGRAM.

(a) IN GENERAL.—The Secretary of Agriculture (hereinafter in
this section referred to as the ‘‘Secretary’’) shall assure the coordination of the responsibilities of the Department of Agriculture related to minor uses of pesticides, including—
(1) carrying out the Inter-Regional Project Number 4 (IR–
4) as described in section 2 of Public Law 89–106 (7 U.S.C.
450i(e)) and the national pesticide resistance monitoring program established under section 1651 of the Food, Agriculture,
Conservation, and Trade Act of 1990 (7 U.S.C. 5882);
(2) supporting integrated pest management research;
(3) consulting with growers to develop data for minor uses;
and
(4) providing assistance for minor use registrations, tolerances, and reregistrations with the Environmental Protection
Agency.
(b)(1) MINOR USE PESTICIDE DATA.—
(A) GRANT AUTHORITY.—The Secretary, in consultation
with the Administrator, shall establish a program to make
grants for the development of data to support minor use pesticide registrations and reregistrations. The amount of any
such grant shall not exceed 1⁄2 of the cost of the project for
which the grant is made.
(B) APPLICANTS.—Any person who wants to develop data to
support minor use pesticide registrations and reregistrations
may apply for a grant under subparagraph (A). Priority shall
be given to an applicant for such a grant who does not directly

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receive funds from the sale of pesticides registered for minor
uses.
(C) DATA OWNERSHIP.—Any data that is developed under
a grant under subparagraph (A) shall be jointly owned by the
Department of Agriculture and the person who received the
grant. Such a person shall enter into an agreement with the
Secretary under which such person shall share any fee paid to
such person under section 3(c)(1)(F).
(2) MINOR USE PESTICIDE DATA REVOLVING FUND.—
(A) ESTABLISHMENT.—There is established in the Treasury
of the United States a revolving fund to be known as the Minor
Use Pesticide Data Revolving Fund. The Fund shall be available without fiscal year limitation to carry out the authorized
purposes of this subsection.
(B) CONTENTS OF THE FUND.—There shall be deposited in
the Fund—
(i) such amounts as may be appropriated to support
the purposes of this subsection; and
(ii) fees collected by the Secretary for any data developed under a grant under paragraph (1)(A).
(C) AUTHORIZATIONS OF APPROPRIATIONS.—There are authorized to be appropriated for each fiscal year to carry out the
purposes of this subsection $10,000,000 to remain available
until expended.
SEC. 33. ø7 U.S.C. 136w–8¿ PESTICIDE REGISTRATION SERVICE FEES.

(a) DEFINITION OF COSTS.—In this section, the term ‘‘costs’’,
when used with respect to review and decisionmaking pertaining to
an application for which registration service fees are paid under
this section, means—
(1) costs to the extent that—
(A) officers and employees provide direct support for
the review and decisionmaking for covered pesticide applications, associated tolerances, and corresponding risk and
benefits information and analyses;
(B) persons and organizations under contract with the
Administrator engage in the review of the applications,
and corresponding risk and benefits information and assessments; and
(C) advisory committees and other accredited persons
or organizations, on the request of the Administrator, engage in the peer review of risk or benefits information associated with covered pesticide applications;
(2) costs of management of information, and the acquisition, maintenance, and repair of computer and telecommunication resources (including software), used to support review of
pesticide applications, associated tolerances, and corresponding
risk and benefits information and analyses; and
(3) costs of collecting registration service fees under subsections (b) and (c) and reporting, auditing, and accounting
under this section.
(b) FEES.—
(1) IN GENERAL.—Effective beginning on the effective date
of the Pesticide Registration Improvement Act of 2003, the Ad-

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Sec. 33

ministrator shall assess and collect covered pesticide registration service fees in accordance with this section.
(2) COVERED PESTICIDE REGISTRATION APPLICATIONS.—
(A) IN GENERAL.—An application for the registration of
a pesticide covered by this Act that is received by the Administrator on or after the effective date of the Pesticide
Registration Improvement Act of 2003 shall be subject to
a registration service fee under this section.
(B) EXISTING APPLICATIONS.—
(i) IN GENERAL.—Subject to clause (ii), an application for the registration of a pesticide that was submitted to the Administrator before the effective date of
the Pesticide Registration Improvement Act of 2003
and is pending on that effective date shall be subject
to a service fee under this section if the application is
for the registration of a new active ingredient that is
not listed in the Registration Division 2003 Work Plan
of the Office of Pesticide Programs of the Environmental Protection Agency.
(ii) TOLERANCE OR EXEMPTION FEES.—The amount
of any fee otherwise payable for an application described in clause (i) under this section shall be reduced
by the amount of any fees paid to support the related
petition for a pesticide tolerance or exemption under
the Federal Food, Drug, and Cosmetic Act (21 U.S.C.
301 et seq.).
(C) DOCUMENTATION.—An application subject to a registration service fee under this section shall be submitted
with documentation certifying—
(i) payment of the registration service fee; or
(ii) payment of at least 25 percent of the registration service fee and a request for a waiver from or reduction of the remaining amount of the registration
service fee.
(D) PAYMENT.—The registration service fee required
under this subsection shall be due upon submission of the
application.
(E) APPLICATIONS SUBJECT TO ADDITIONAL FEES.—An
application may be subject to additional fees if—
(i) the applicant identified the incorrect registration service fee and decision review period;
(ii) after review of a waiver request, the Administrator denies the waiver request; or
(iii) after review of the application, the Administrator determines that a different registration service
fee and decision review period apply to the application.
(F) EFFECT OF FAILURE TO PAY FEES.—The Administrator shall reject any application submitted without the
required registration service fee.
(G) NON-REFUNDABLE PORTION OF FEES.—
(i) IN GENERAL.—The Administrator shall retain
25 percent of the applicable registration service fee.
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(ii) LIMITATION.—Any waiver, refund, credit or
other reduction in the registration service fee shall not
exceed 75 percent of the registration service fee.
(H) COLLECTION OF UNPAID FEES.—In any case in
which the Administrator does not receive payment of a
registration service fee (or applicable portion of the registration service fee) by the date that is 30 days after the
fee is due, the fee shall be treated as a claim of the United
States Government subject to subchapter II of chapter 37
of title 31, United States Code.
(3) SCHEDULE OF COVERED APPLICATIONS AND REGISTRATION SERVICE FEES.—Subject to paragraph (6), the schedule of
covered pesticide registration applications and corresponding
registration service fees shall be as follows:
TABLE 1. — REGISTRATION DIVISION — NEW ACTIVE INGREDIENTS

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

R010

1

New Active Ingredient, Food use
(2) (3)

24

569,221

R020

2

New Active Ingredient, Food use;
reduced risk (2) (3)

18

569,221

R040

3

New Active Ingredient, Food use;
Experimental Use Permit application; establish temporary tolerance; submitted before application for registration; credit
45% of fee toward new active
ingredient application that follows (3)

18

419,502

R060

4

New Active Ingredient, Non-food
use; outdoor (2) (3)

21

395,467

R070

5

New Active Ingredient, Non-food
use; outdoor; reduced risk (2)
(3)

16

395,467

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TABLE 1. — REGISTRATION DIVISION — NEW ACTIVE INGREDIENTS—Continued

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

R090

6

New Active Ingredient, Non-food
use; outdoor; Experimental Use
Permit application; submitted
before application for registration; credit 45% of fee toward
new active ingredient (3)

16

293,596

R110

7

New Active Ingredient, Non-food
use; indoor (2) (3)

20

219,949

R120

8

New Active Ingredient, Non-food
use; indoor; reduced risk (2) (3)

14

219,949

R121

9

New Active Ingredient, Non-food
use; indoor; Experimental Use
Permit application; submitted
before application for registration; credit 45% of fee toward
new active ingredient application that follows (3)

18

165,375

R122

10

Enriched isomer(s) of registered
mixed-isomer active ingredient
(2) (3)

18

287,643

R123

11

New Active Ingredient, Seed treatment only; includes agricultural
and non-agricultural seeds;
residues not expected in raw
agricultural commodities (2) (3)

18

427,991

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TABLE 1. — REGISTRATION DIVISION — NEW ACTIVE INGREDIENTS—Continued

EPA
No.

New
CR
No.

R125
New

12

Action

New Active Ingredient, Seed treatment; Experimental Use Permit
application; submitted before
application for registration;
credit 45% of fee toward new
active ingredient application
that follows (3)

Decision
Review
Time
(Months)
(1)
16

Registration
Service Fee
($)
293,596

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
(2) All requests for new uses (food and/or nonfood) contained in any application for
a new active ingredient or a first food use are covered by the base fee for that new
active ingredient or first food use application and retain the same decision time review period as the new active ingredient or first food use application. The application
must be received by the agency in one package. The base fee for the category covers a
maximum of five new products. Each application for an additional new product registration and new inert approval that is submitted in the new active ingredient application package or first food use application package is subject to the registration
service fee for a new product or a new inert approval. All such associated applications
that are submitted together will be subject to the new active ingredient or first food
use decision review time. In the case of a new active ingredient application, until that
new active ingredient is approved, any subsequent application for another new product
containing the same active ingredient or an amendment to the proposed labeling will
be deemed a new active ingredient application, subject to the registration service fee
and decision review time for a new active ingredient. In the case of a first food use
application, until that first food use is approved, any subsequent application for an
additional new food use or uses will be subject to the registration service fee and decision review time for a first food use. Any information that (a) was neither requested
nor required by the Agency, and (b) is submitted by the applicant at the applicant’s
initiative to support the application after completion of the technical deficiency screening, and (c) is not itself a covered registration application, must be assessed 25% of
the full registration service fee for the new active ingredient or first food use application.

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(3) Where the action involves approval of a new or amended label, on or before the
end date of the decision review time, the Agency shall provide to the applicant a draft
accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it
be issued as the accepted final Agency-stamped label; or (b) does not agree to one or
more of the terms of the draft accepted label as amended by the Agency and requests
additional time to resolve the difference(s); or (c) withdraws the application without
prejudice for subsequent resubmission, but forfeits the associated registration service
fee. For cases described in (b), the applicant shall have up to 30 calendar days to
reach agreement with the Agency on the final terms of the Agency-accepted label. If
the applicant agrees to all of the terms of the accepted label as in (a), including upon
resolution of differences in (b), the Agency shall provide an accepted final Agencystamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency.
TABLE 2. — REGISTRATION DIVISION — NEW USES

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

R130

13

First food use; indoor; food/food
handling (2) (3)

21

173,644

R140

14

Additional food use; Indoor; food/
food handling (3) (4)

15

40,518

R150

15

First food use (2) (3)

21

239,684

R160

16

First food use; reduced risk (2) (3)

16

239,684

R170

17

Additional food use (3) (4)

15

59,976

R175
New

18

Additional food uses covered within a crop group resulting from
the conversion of existing approved crop group(s) to one or
more revised crop groups. (3)
(4)

10

59,976

R180

19

Additional food use; reduced risk
(3) (4)

10

59,976

Action

Registration
Service Fee
($)

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TABLE 2. — REGISTRATION DIVISION — NEW USES—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

R190

20

Additional food uses; 6 or more
submitted in one application
(3) (4)

15

359,856

R200

21

Additional food uses; 6 or more
submitted in one application;
reduced risk (3) (4)

10

359,856

R210

22

Additional food use; Experimental
Use Permit application; establish temporary tolerance; no
credit toward new use registration (3) (4)

12

44,431

R220

23

Additional food use; Experimental
Use Permit application; crop
destruct basis; no credit toward
new use registration (3) (4)

6

17,993

R230

24

Additional use; non-food; outdoor
(3) (4)

15

23,969

R240

25

Additional use; non-food; outdoor;
reduced risk (3) (4)

10

23,969

R250

26

Additional use; non-food; outdoor;
Experimental Use Permit application; no credit toward new
use registration (3) (4)

6

17,993

R251
New

27

Experimental Use Permit application which requires no changes
to the tolerance(s); non-crop
destruct basis (3)

8

17,993

R260

28

New use; non-food; indoor (3) (4)

12

11,577

Action

Registration
Service Fee
($)

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Sec. 33

TABLE 2. — REGISTRATION DIVISION — NEW USES—Continued
Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

R270

29

New use; non-food; indoor; reduced risk (3) (4)

9

11,577

R271

30

New use; non-food; indoor; Experimental Use Permit application;
no credit toward new use registration (3) (4)

6

8,820

R273

31

Additional use; seed treatment;
limited uptake into raw agricultural commodities; includes
crops with established tolerances (e.g., for soil or foliar
application); includes food or
non-food uses (3) (4)

12

45,754

R274

32

Additional uses; seed treatment
only; 6 or more submitted in
one application; limited uptake
into raw agricultural commodities; includes crops with established tolerances (e.g., for
soil or foliar application); includes food and/or non-food
uses (3) (4)

12

274,523

Action

Registration
Service Fee
($)

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.

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(2) All requests for new uses (food and/or nonfood) contained in any application for
a new active ingredient or a first food use are covered by the base fee for that new
active ingredient or first food use application and retain the same decision time review period as the new active ingredient or first food use application. The application
must be received by the agency in one package. The base fee for the category covers a
maximum of five new products. Each application for an additional new product registration and new inert approval that is submitted in the new active ingredient application package or first food use application package is subject to the registration
service fee for a new product or a new inert approval. All such associated applications
that are submitted together will be subject to the new active ingredient or first food
use decision review time. In the case of a new active ingredient application, until that
new active ingredient is approved, any subsequent application for another new product
containing the same active ingredient or an amendment to the proposed labeling will
be deemed a new active ingredient application, subject to the registration service fee
and decision review time for a new active ingredient. In the case of a first food use
application, until that first food use is approved, any subsequent application for an
additional new food use or uses will be subject to the registration service fee and decision review time for a first food use. Any information that (a) was neither requested
nor required by the Agency, and (b) is submitted by the applicant at the applicant’s
initiative to support the application after completion of the technical deficiency screening, and (c) is not itself a covered registration application, must be assessed 25% of
the full registration service fee for the new active ingredient or first food use application.
(3) Where the action involves approval of a new or amended label, on or before the
end date of the decision review time, the Agency shall provide to the applicant a draft
accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it
be issued as the accepted final Agency-stamped label; or (b) does not agree to one or
more of the terms of the draft accepted label as amended by the Agency and requests
additional time to resolve the difference(s); or (c) withdraws the application without
prejudice for subsequent resubmission, but forfeits the associated registration service
fee. For cases described in (b), the applicant shall have up to 30 calendar days to
reach agreement with the Agency on the final terms of the Agency-accepted label. If
the applicant agrees to all of the terms of the accepted label as in (a), including upon
resolution of differences in (b), the Agency shall provide an accepted final Agencystamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency.

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Sec. 33

(4) Amendment applications to add the new use(s) to registered product labels are
covered by the base fee for the new use(s). All items in the covered application must
be submitted together in one package. Each application for an additional new product
registration and new inert approval(s) that is submitted in the new use application
package is subject to the registration service fee for a new product or a new inert approval. However, if a new use application only proposes to register the new use for a
new product and there are no amendments in the application, then review of one new
product application is covered by the new use fee. All such associated applications
that are submitted together will be subject to the new use decision review time. Any
application for a new product or an amendment to the proposed labeling (a) submitted
subsequent to submission of the new use application and (b) prior to conclusion of its
decision review time and (c) containing the same new uses, will be deemed a separate new-use application, subject to a separate registration service fee and new decision review time for a new use. If the new-use application includes non-food (indoor
and/or outdoor), and food (outdoor and/or indoor) uses, the appropriate fee is due for
each type of new use and the longest decision review time applies to all of the new
uses requested in the application. Any information that (a) was neither requested nor
required by the Agency, and (b) is submitted by the applicant at the applicant’s initiative to support the application after completion of the technical deficiency screen, and
(c) is not itself a covered registration application, must be assessed 25% of the full
registration service fee for the new use application.
TABLE 3. — REGISTRATION DIVISION — IMPORT AND OTHER TOLERANCES

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

R280

33

Establish import tolerance; new
active ingredient or first food
use (2)

21

289,407

R290

34

Establish import tolerance; additional food use

15

57,882

R291

35

Establish import tolerances; additional food uses; 6 or more
crops submitted in one petition

15

347,288

R292

36

Amend an established tolerance
(e.g., decrease or increase); domestic or import; applicant-initiated

11

41,124

Action

Registration
Service Fee
($)

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TABLE 3. — REGISTRATION DIVISION — IMPORT AND OTHER TOLERANCES—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

R293

37

Establish tolerance(s) for inadvertent residues in one crop;
applicant-initiated

12

48,510

R294

38

Establish tolerances for inadvertent residues; 6 or more
crops submitted in one application; applicant-initiated

12

291,060

R295

39

Establish tolerance(s) for residues
in one rotational crop in response to a specific rotational
crop application; applicant-initiated

15

59,976

R296

40

Establish tolerances for residues
in rotational crops in response
to a specific rotational crop petition; 6 or more crops submitted in one application; applicant-initiated

15

359,856

R297
New

41

Amend 6 or more established tolerances (e.g., decrease or increase) in one petition; domestic or import; applicant-initiated

11

246,744

R298
New

42

Amend an established tolerance
(e.g., decrease or increase); domestic or import; submission of
amended labels (requiring
science review) in addition to
those associated with the
amended tolerance; applicantinitiated (3)

13

53,120

Action

Registration
Service Fee
($)

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TABLE 3. — REGISTRATION DIVISION — IMPORT AND OTHER TOLERANCES—Continued

EPA
No.

New
CR
No.

R299
New

43

Action

Amend 6 or more established tolerances (e.g., decrease or increase); domestic or import;
submission of amended labels
(requiring science review) in
addition to those associated
with the amended tolerance;
applicant-initiated (3)

Decision
Review
Time
(Months)
(1)
13

Registration
Service Fee
($)
258,740

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
(2) All requests for new uses (food and/or nonfood) contained in any application for
a new active ingredient or a first food use are covered by the base fee for that new
active ingredient or first food use application and retain the same decision time review period as the new active ingredient or first food use application. The application
must be received by the agency in one package. The base fee for the category covers a
maximum of five new products. Each application for an additional new product registration and new inert approval that is submitted in the new active ingredient application package or first food use application package is subject to the registration
service fee for a new product or a new inert approval. All such associated applications
that are submitted together will be subject to the new active ingredient or first food
use decision review time. In the case of a new active ingredient application, until that
new active ingredient is approved, any subsequent application for another new product
containing the same active ingredient or an amendment to the proposed labeling will
be deemed a new active ingredient application, subject to the registration service fee
and decision review time for a new active ingredient. In the case of a first food use
application, until that first food use is approved, any subsequent application for an
additional new food use or uses will be subject to the registration service fee and decision review time for a first food use. Any information that (a) was neither requested
nor required by the Agency, and (b) is submitted by the applicant at the applicant’s
initiative to support the application after completion of the technical deficiency screening, and (c) is not itself a covered registration application, must be assessed 25% of
the full registration service fee for the new active ingredient or first food use application.

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FIFRA

110

(3) Where the action involves approval of a new or amended label, on or before the
end date of the decision review time, the Agency shall provide to the applicant a draft
accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it
be issued as the accepted final Agency-stamped label; or (b) does not agree to one or
more of the terms of the draft accepted label as amended by the Agency and requests
additional time to resolve the difference(s); or (c) withdraws the application without
prejudice for subsequent resubmission, but forfeits the associated registration service
fee. For cases described in (b), the applicant shall have up to 30 calendar days to
reach agreement with the Agency on the final terms of the Agency-accepted label. If
the applicant agrees to all of the terms of the accepted label as in (a), including upon
resolution of differences in (b), the Agency shall provide an accepted final Agencystamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency.
TABLE 4. — REGISTRATION DIVISION — NEW PRODUCTS

September 28, 2012

EPA
No.

New
CR
No.

R300

44

Action

New product; or similar combination product (already registered)
to an identical or substantially
similar in composition and use
to a registered product; registered source of active ingredient; no data review on acute
toxicity, efficacy or CRP – only
product chemistry data; cite-all
data citation, or selective data
citation where applicant owns
all required data, or applicant
submits specific authorization
letter from data owner. Category also includes 100% repackage of registered end-use
or manufacturing-use product
that requires no data submission nor data matrix. (2) (3)

Decision
Review
Time
(Months)
(1)
4

Registration
Service Fee
($)
1,434

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TABLE 4. — REGISTRATION DIVISION — NEW PRODUCTS—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

R301

45

New product; or similar combination product (already registered)
to an identical or substantially
similar in composition and use
to a registered product; registered source of active ingredient; selective data citation
only for data on product chemistry and/or acute toxicity and/
or public health pest efficacy,
where applicant does not own
all required data and does not
have a specific authorization
letter from data owner. (2) (3)

4

1,720

R310

46

New end-use or manufacturinguse product with registered
source(s) of active ingredient(s); includes products containing two or more registered
active ingredients previously
combined in other registered
products; requires review of
data package within RD only;
includes data and/or waivers of
data for only:
∑ product chemistry and/or
∑ acute toxicity and/or
∑ public health pest efficacy and/
or
∑ child resistant packaging. (2)
(3)

7

4,807

Action

Registration
Service Fee
($)

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FIFRA

112

TABLE 4. — REGISTRATION DIVISION — NEW PRODUCTS—Continued

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

R314
New

47

New end use product containing
two or more registered active
ingredients never before registered as this combination in
a formulated product; new
product label is identical or
substantially similar to the labels of currently registered
products which separately contain the respective component
active ingredients; requires review of data package within RD
only; includes data and/or
waivers of data for only:
∑ product chemistry and/or
∑ acute toxicity and/or
∑ public health pest efficacy and/
or
∑ child resistant packaging. (2)
(3)

8

6,009

R315
New

48

New end-use non-food animal
product with submission of two
or more target animal safety
studies; includes data and/or
waivers of data for only:
∑ product chemistry and/or
∑ acute toxicity and/or
∑ public health pest efficacy and/
or
∑ animal safety studies and/or
∑ child resistant packaging (2)
(3)

9

8,000

R320

49

New product; new physical form;
requires data review in science
divisions (2) (3)

12

11,996

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TABLE 4. — REGISTRATION DIVISION — NEW PRODUCTS—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

R331

50

New product; repack of identical
registered end-use product as a
manufacturing-use product;
same registered uses only (2)
(3)

3

2,294

R332

51

New manufacturing-use product;
registered active ingredient; unregistered source of active ingredient; submission of completely new generic data package; registered uses only; requires review in RD and
science divisions (2) (3)

24

256,883

R333
New

52

New product; MUP or End use
product with unregistered
source of active ingredient; requires science data review; new
physical form; etc. Cite-all or
selective data citation where
applicant owns all required
data. (2) (3)

10

17,993

Action

Registration
Service Fee
($)

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FIFRA

114

TABLE 4. — REGISTRATION DIVISION — NEW PRODUCTS—Continued

EPA
No.

New
CR
No.

R334
New

53

Action

New product; MUP or End use
product with unregistered
source of the active ingredient;
requires science data review;
new physical form; etc. Selective data citation. (2) (3)

Decision
Review
Time
(Months)
(1)
11

Registration
Service Fee
($)
17,993

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
*ERR93*(2) An application for a new end-use product using a source of active ingredient that (a) is not yet registered but (b) has an application pending with the
Agency for review, will be considered an application for a new product with an unregistered source of active ingredient.
(3) Where the action involves approval of a new or amended label, on or before the
end date of the decision review time, the Agency shall provide to the applicant a draft
accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it
be issued as the accepted final Agency-stamped label; or (b) does not agree to one or
more of the terms of the draft accepted label as amended by the Agency and requests
additional time to resolve the difference(s); or (c) withdraws the application without
prejudice for subsequent resubmission, but forfeits the associated registration service
fee. For cases described in (b), the applicant shall have up to 30 calendar days to
reach agreement with the Agency on the final terms of the Agency-accepted label. If
the applicant agrees to all of the terms of the accepted label as in (a), including upon
resolution of differences in (b), the Agency shall provide an accepted final Agencystamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency.

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Sec. 33

TABLE 5. — REGISTRATION DIVISION — AMENDMENTS TO REGISTRATION

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

R340

54

Amendment requiring data review
within RD (e.g., changes to
precautionary label statements)
(2) (3)

4

3,617

R345
New

55

Amending non-food animal product that includes submission of
target animal safety data; previously registered (2) (3)

7

8,000

R350

56

Amendment requiring data review
in science divisions (e.g.,
changes to REI, or PPE, or PHI,
or use rate, or number of applications; or add aerial application; or modify GW/SW advisory
statement) (2) (3)

9

11,996

R351
New

57

Amendment adding a new unregistered source of active ingredient. (2) (3)

8

11,996

R352
New

58

Amendment adding already approved uses; selective method
of support; does not apply if
the applicant owns all cited
data (2) (3)

8

11,996

Action

Registration
Service Fee
($)

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FIFRA

116

TABLE 5. — REGISTRATION DIVISION — AMENDMENTS TO REGISTRATION—Continued

EPA
No.

New
CR
No.

R371

59

Action

Amendment to Experimental Use
Permit; (does not include extending a permit’s time period)
(3)

Decision
Review
Time
(Months)
(1)
6

Registration
Service Fee
($)
9,151

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
*ERR93*(2) (a) EPA-initiated amendments shall not be charged registration service
fees. (b) Registrant-initiated fast-track amendments are to be completed within the
timelines specified in FIFRA Section 3(c)(3)(B) and are not subject to registration service fees. (c) Registrant-initiated fast-track amendments handled by the Antimicrobials
Division are to be completed within the timelines specified in FIFRA Section 3(h) and
are not subject to registration service fees. (d) Registrant initiated amendments submitted by notification under PR Notices, such as PR Notice 98–10, continue under PR
Notice timelines and are not subject to registration service fees. (e) Submissions with
data and requiring data review are subject to registration service fees.
(3) Where the action involves approval of a new or amended label, on or before the
end date of the decision review time, the Agency shall provide to the applicant a draft
accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it
be issued as the accepted final Agency-stamped label; or (b) does not agree to one or
more of the terms of the draft accepted label as amended by the Agency and requests
additional time to resolve the difference(s); or (c) withdraws the application without
prejudice for subsequent resubmission, but forfeits the associated registration service
fee. For cases described in (b), the applicant shall have up to 30 calendar days to
reach agreement with the Agency on the final terms of the Agency-accepted label. If
the applicant agrees to all of the terms of the accepted label as in (a), including upon
resolution of differences in (b), the Agency shall provide an accepted final Agencystamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency.

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Sec. 33

TABLE 6. — REGISTRATION DIVISION — OTHER ACTIONS
Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

R124

60

Conditional Ruling on
Preapplication Study Waivers;
applicant-initiated

6

2,294

R272

61

Review of Study Protocol applicant-initiated; excludes DART,
pre-registration conference,
Rapid Response review, DNT
protocol review, protocol needing HSRB review

3

2,294

R275
New

62

Rebuttal of agency reviewed protocol, applicant initiated

3

2,294

R370

63

Cancer reassessment; applicantinitiated

18

179,818

Action

Registration
Service Fee
($)

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
TABLE 7. — ANTIMICROBIALS DIVISION — NEW ACTIVE INGREDIENTS

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

A380

64

Food use; establish tolerance exemption (2) (3)

24

104,187

A390

65

Food use; establish tolerance (2)
(3)

24

173,644

A400

66

Non-food use; outdoor; FIFRA
§2(mm) uses (2) (3)

18

86,823

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FIFRA

118

TABLE 7. — ANTIMICROBIALS DIVISION — NEW ACTIVE INGREDIENTS—Continued

EPA
No.

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

A410

67

Non-food use; outdoor; uses other
than FIFRA §2(mm) (2) (3)

21

173,644

A420

68

Non-food use; indoor; FIFRA
§2(mm) uses (2) (3)

18

57,882

A430

69

Non-food use; indoor; uses other
than FIFRA §2(mm) (2) (3)

20

86,823

A431

70

Non-food use; indoor; low-risk,
low-toxicity food-grade active
ingredient(s); efficacy testing
for public health claims required under GLP and following
DIS/TSS or AD-approved study
protocol (2) (3)

12

60,638

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
(2) All requests for new uses (food and/or nonfood) contained in any application for
a new active ingredient or a first food use are covered by the base fee for that new
active ingredient or first food use application and retain the same decision time review period as the new active ingredient or first food use application. The application
must be received by the agency in one package. The base fee for the category covers a
maximum of five new products. Each application for an additional new product registration and new inert approval that is submitted in the new active ingredient application package or first food use application package is subject to the registration
service fee for a new product or a new inert approval. All such associated applications
that are submitted together will be subject to the new active ingredient or first food
use decision review time. In the case of a new active ingredient application, until that
new active ingredient is approved, any subsequent application for another new product
containing the same active ingredient or an amendment to the proposed labeling will
be deemed a new active ingredient application, subject to the registration service fee
and decision review time for a new active ingredient. In the case of a first food use
application, until that first food use is approved, any subsequent application for an
additional new food use or uses will be subject to the registration service fee and decision review time for a first food use. Any information that (a) was neither requested
nor required by the Agency, and (b) is submitted by the applicant at the applicant’s
initiative to support the application after completion of the technical deficiency screening, and (c) is not itself a covered registration application, must be assessed 25% of
the full registration service fee for the new active ingredient or first food use application.
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Sec. 33

(3) Where the action involves approval of a new or amended label, on or before the
end date of the decision review time, the Agency shall provide to the applicant a draft
accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it
be issued as the accepted final Agency-stamped label; or (b) does not agree to one or
more of the terms of the draft accepted label as amended by the Agency and requests
additional time to resolve the difference(s); or (c) withdraws the application without
prejudice for subsequent resubmission, but forfeits the associated registration service
fee. For cases described in (b), the applicant shall have up to 30 calendar days to
reach agreement with the Agency on the final terms of the Agency-accepted label. If
the applicant agrees to all of the terms of the accepted label as in (a), including upon
resolution of differences in (b), the Agency shall provide an accepted final Agencystamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency.
TABLE 8. — ANTIMICROBIALS DIVISION — NEW USES

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

A440

71

First food use; establish tolerance
exemption (2) (3) (4)

21

28,942

A450

72

First food use; establish tolerance
(2) (3) (4)

21

86,823

A460

73

Additional food use; establish tolerance exemption (3) (4) (5)

15

11,577

A470

74

Additional food use; establish tolerance (3) (4) (5)

15

28,942

A471
New

75

Additional food uses; establish
tolerances; 6 or more submitted
in one application (3) (4) (5)

15

173,652

A480

76

Additional use; non-food; outdoor;
FIFRA §2(mm) uses (4) (5)

9

17,365

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120

TABLE 8. — ANTIMICROBIALS DIVISION — NEW USES—Continued

EPA
No.

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

A481
New

77

Additional non-food outdoor uses;
FIFRA §2(mm) uses; 6 or more
submitted in one application
(4) (5)

9

104,190

A490

78

Additional use; non-food; outdoor;
uses other than FIFRA §2(mm)
(4) (5)

15

28,942

A491
New

79

Additional non-food; outdoor; uses
other than FIFRA §2(mm); 6 or
more submitted in one application (4) (5)

15

173,652

A500

80

Additional use; non-food, indoor,
FIFRA §2(mm) uses (4) (5)

9

11,577

A501
New

81

Additional non-food; indoor; FIFRA
§2(mm) uses; 6 or more submitted in one application (4)
(5)

9

69,462

A510

82

Additional use; non-food; indoor;
uses other than FIFRA §2(mm)
(4) (5)

12

11,577

A511
New

83

Additional non-food; indoor; uses
other than FIFRA §2(mm); 6 or
more submitted in one application (4) (5)

12

69,462

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.

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Sec. 33

(2) All requests for new uses (food and/or nonfood) contained in any application for
a new active ingredient or a first food use are covered by the base fee for that new
active ingredient or first food use application and retain the same decision time review period as the new active ingredient or first food use application. The application
must be received by the agency in one package. The base fee for the category covers a
maximum of five new products. Each application for an additional new product registration and new inert approval that is submitted in the new active ingredient application package or first food use application package is subject to the registration
service fee for a new product or a new inert approval. All such associated applications
that are submitted together will be subject to the new active ingredient or first food
use decision review time. In the case of a new active ingredient application, until that
new active ingredient is approved, any subsequent application for another new product
containing the same active ingredient or an amendment to the proposed labeling will
be deemed a new active ingredient application, subject to the registration service fee
and decision review time for a new active ingredient. In the case of a first food use
application, until that first food use is approved, any subsequent application for an
additional new food use or uses will be subject to the registration service fee and decision review time for a first food use. Any information that (a) was neither requested
nor required by the Agency, and (b) is submitted by the applicant at the applicant’s
initiative to support the application after completion of the technical deficiency screening, and (c) is not itself a covered registration application, must be assessed 25% of
the full registration service fee for the new active ingredient or first food use application.
(3) If EPA data rules are amended to newly require clearance under section 408 of
the FFDCA for an ingredient of an antimicrobial product where such ingredient was not
previously subject to such a clearance, then review of the data for such clearance of
such product is not subject to a registration service fee for the tolerance action for
two years from the effective date of the rule.
(4) Where the action involves approval of a new or amended label, on or before the
end date of the decision review time, the Agency shall provide to the applicant a draft
accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it
be issued as the accepted final Agency-stamped label; or (b) does not agree to one or
more of the terms of the draft accepted label as amended by the Agency and requests
additional time to resolve the difference(s); or (c) withdraws the application without
prejudice for subsequent resubmission, but forfeits the associated registration service
fee. For cases described in (b), the applicant shall have up to 30 calendar days to
reach agreement with the Agency on the final terms of the Agency-accepted label. If
the applicant agrees to all of the terms of the accepted label as in (a), including upon
resolution of differences in (b), the Agency shall provide an accepted final Agencystamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency.

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122

(5) Amendment applications to add the new use(s) to registered product labels are
covered by the base fee for the new use(s). All items in the covered application must
be submitted together in one package. Each application for an additional new product
registration and new inert approval(s) that is submitted in the new use application
package is subject to the registration service fee for a new product or a new inert approval. However, if a new use application only proposes to register the new use for a
new product and there are no amendments in the application, then review of one new
product application is covered by the new use fee. All such associated applications
that are submitted together will be subject to the new use decision review time. Any
application for a new product or an amendment to the proposed labeling (a) submitted
subsequent to submission of the new use application and (b) prior to conclusion of its
decision review time and (c) containing the same new uses, will be deemed a separate new-use application, subject to a separate registration service fee and new decision review time for a new use. If the new-use application includes non-food (indoor
and/or outdoor), and food (outdoor and/or indoor) uses, the appropriate fee is due for
each type of new use and the longest decision review time applies to all of the new
uses requested in the application. Any information that (a) was neither requested nor
required by the Agency, and (b) is submitted by the applicant at the applicant’s initiative to support the application after completion of the technical deficiency screen, and
(c) is not itself a covered registration application, must be assessed 25% of the full
registration service fee for the new use application.
TABLE 9. — ANTIMICROBIALS DIVISION — NEW PRODUCTS AND AMENDMENTS

EPA
No.

A530

September 28, 2012

New
CR
No.
84

Action

New product; identical or substantially similar in composition
and use to a registered product; no data review or only
product chemistry data; cite-all
data citation, or selective data
citation when applicant owns
all required data, or applicant
submits specific authorization
letter for data owner. Category
also includes 100% re-package
of registered end-use or manufacturing-use product that requires no data submission nor
data matrix. (2) (3)

Decision
Review
Time
(Months)
(1)
4

Registration
Service Fee
($)
1,159

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Sec. 33

TABLE 9. — ANTIMICROBIALS DIVISION — NEW PRODUCTS AND AMENDMENTS—
Continued

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

A531

85

New product; identical or substantially similar in composition
and use to a registered product; registered source of active
ingredient: selective data citation only for data on product
chemistry and/or acute toxicity
and/or public health pest efficacy, where applicant does not
own all required data and does
not have a specific authorization letter from data owner. (2)
(3)

4

1,654

A532

86

New product; identical or substantially similar in composition
and use to a registered product; registered active ingredient; unregistered source of
active ingredient; cite-all data
citation except for product
chemistry; product chemistry
data submitted (2) (3)

5

4,631

A540

87

New end use product; FIFRA
§2(mm) uses only (2) (3)

5

4,631

A550

88

New end-use product; uses other
than FIFRA §2(mm); non-FQPA
product (2) (3)

7

4,631

A560

89

New manufacturing-use product;
registered active ingredient; selective data citation (2) (3)

12

17,365

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124

TABLE 9. — ANTIMICROBIALS DIVISION — NEW PRODUCTS AND AMENDMENTS—
Continued

EPA
No.

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

A570

90

Label amendment requiring data
review (3) (4)

4

3,474

A572
New

91

New Product or amendment requiring data review for risk assessment by Science Branch
(e.g., changes to REI, or PPE, or
use rate) (2) (3) (4)

9

11,996

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
(2) An application for a new end-use product using a source of active ingredient
that (a) is not yet registered but (b) has an application pending with the Agency for
review, will be considered an application for a new product with an unregistered
source of active ingredient.
(3) Where the action involves approval of a new or amended label, on or before the
end date of the decision review time, the Agency shall provide to the applicant a draft
accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it
be issued as the accepted final Agency-stamped label; or (b) does not agree to one or
more of the terms of the draft accepted label as amended by the Agency and requests
additional time to resolve the difference(s); or (c) withdraws the application without
prejudice for subsequent resubmission, but forfeits the associated registration service
fee. For cases described in (b), the applicant shall have up to 30 calendar days to
reach agreement with the Agency on the final terms of the Agency-accepted label. If
the applicant agrees to all of the terms of the accepted label as in (a), including upon
resolution of differences in (b), the Agency shall provide an accepted final Agencystamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency.
(4) (a) EPA-initiated amendments shall not be charged registration service fees. (b)
Registrant-initiated fast-track amendments are to be completed within the timelines
specified in FIFRA Section 3(c)(3)(B) and are not subject to registration service fees.
(c) Registrant-initiated fast-track amendments handled by the Antimicrobials Division
are to be completed within the timelines specified in FIFRA Section 3(h) and are not
subject to registration service fees. (d) Registrant initiated amendments submitted by
notification under PR Notices, such as PR Notice 98–10, continue under PR Notice
timelines and are not subject to registration service fees. (e) Submissions with data
and requiring data review are subject to registration service fees.

September 28, 2012

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FIFRA

Sec. 33

TABLE 10. — ANTIMICROBIALS DIVISION — EXPERIMENTAL USE PERMITS AND OTHER
TYPE OF ACTIONS

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

A520

92

Experimental Use Permit application, Non-Food Use (2)

9

5,789

A521

93

Review of public health efficacy
study protocol within AD, per
AD Internal Guidance for the
Efficacy Protocol Review Process; Code will also include review of public health efficacy
study protocol and data review
for devices making pesticidal
claims; applicant-initiated; Tier
1

3

2,250

A522

94

Review of public health efficacy
study protocol outside AD by
members of AD Efficacy Protocol Review Expert Panel; Code
will also include review of public health efficacy study protocol and data review for devices making pesticidal claims;
applicant-initiated; Tier 2

12

11,025

A524
New

95

New Active Ingredient, Experimental Use Permit application;
Food Use Requires Tolerance.
Credit 45% of fee toward new
active ingredient application
that follows. (2)

18

138,916

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FIFRA

126

TABLE 10. — ANTIMICROBIALS DIVISION — EXPERIMENTAL USE PERMITS AND OTHER
TYPE OF ACTIONS—Continued

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

A525
New

96

New Active Ingredient, Experimental Use Permit application;
Food Use Requires Tolerance
Exemption. Credit 45% of fee
toward new active ingredient
application that follows. (2)

18

83,594

A526
New

97

New Active Ingredient, Experimental Use Permit application;
Non-Food, Outdoor Use. Credit
45% of fee toward new active
ingredient application that follows. (2)

15

86,823

A527
New

98

New Active Ingredient, Experimental Use Permit application;
Non-Food, Indoor Use. Credit
45% of fee toward new active
ingredient application that follows. (2)

15

58,000

A528
New

99

Experimental Use Permit application, Food Use; Requires Tolerance or Tolerance Exemption (2)

15

20,260

A529
New

100

Amendment to Experimental Use
Permit; requires data review or
risk assessment (2)

9

10,365

A523
New

101

Review of protocol other than a
public health efficacy study
(i.e., Toxicology or Exposure Protocols)

9

11,025

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Sec. 33

TABLE 10. — ANTIMICROBIALS DIVISION — EXPERIMENTAL USE PERMITS AND OTHER
TYPE OF ACTIONS—Continued

EPA
No.

A571
New

New
CR
No.
102

Action

Science reassessment: Cancer
risk, refined ecological risk,
and/or endangered species; applicant-initiated

Decision
Review
Time
(Months)
(1)
18

Registration
Service Fee
($)
86,823

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
*ERR93*(2) Where the action involves approval of a new or amended label, on or
before the end date of the decision review time, the Agency shall provide to the applicant a draft accepted label, including any changes made by the Agency that differ
from the applicant-submitted label and relevant supporting data reviewed by the
Agency. The applicant will notify the Agency that the applicant either (a) agrees to all
of the terms associated with the draft accepted label as amended by the Agency and
requests that it be issued as the accepted final Agency-stamped label; or (b) does not
agree to one or more of the terms of the draft accepted label as amended by the
Agency and requests additional time to resolve the difference(s); or (c) withdraws the
application without prejudice for subsequent resubmission, but forfeits the associated
registration service fee. For cases described in (b), the applicant shall have up to 30
calendar days to reach agreement with the Agency on the final terms of the Agencyaccepted label. If the applicant agrees to all of the terms of the accepted label as in
(a), including upon resolution of differences in (b), the Agency shall provide an accepted final Agency-stamped label to the registrant within 2 business days following the
registrant’s written or electronic confirmation of agreement to the Agency.
TABLE 11. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW ACTIVE INGREDIENTS

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B580

103

New active ingredient; food use;
petition to establish a tolerance
(2)

19

46,305

B590

104

New active ingredient; food use;
petition to establish a tolerance
exemption (2)

17

28,942

Action

Registration
Service Fee
($)

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FIFRA

128

TABLE 11. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW ACTIVE INGREDIENTS—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B600

105

New active ingredient; non-food
use (2)

13

17,365

B610

106

New active ingredient; Experimental Use Permit application;
petition to establish a temporary tolerance or temporary
tolerance exemption

10

11,577

B611
New

107

New active ingredient; Experimental Use Permit application;
petition to establish permanent
tolerance exemption

12

11,577

B612
New

108

New active ingredient; no change
to a permanent tolerance exemption (2)

10

15,918

B613
New

109

New active ingredient; petition to
convert a temporary tolerance
or a temporary tolerance exemption to a permanent tolerance or tolerance exemption (2)

11

15,918

Action

Registration
Service Fee
($)

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FIFRA

Sec. 33

TABLE 11. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW ACTIVE INGREDIENTS—Continued

EPA
No.

New
CR
No.

B620

110

Action

New active ingredient; Experimental Use Permit application;
non-food use including crop destruct

Decision
Review
Time
(Months)
(1)
7

Registration
Service Fee
($)
5,789

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
*ERR93*(2) All requests for new uses (food and/or nonfood) contained in any application for a new active ingredient or a first food use are covered by the base fee for
that new active ingredient or first food use application and retain the same decision
time review period as the new active ingredient or first food use application. The application must be received by the agency in one package. The base fee for the category covers a maximum of five new products. Each application for an additional new
product registration and new inert approval that is submitted in the new active ingredient application package or first food use application package is subject to the registration service fee for a new product or a new inert approval. All such associated applications that are submitted together will be subject to the new active ingredient or
first food use decision review time, except where the new inert approval decision review time is greater than that for the new active ingredient, in which case the associated new active ingredient will be subject to the new inert approval decision review
time. In the case of a new active ingredient application, until that new active ingredient is approved, any subsequent application for another new product containing the
same active ingredient or an amendment to the proposed labeling will be deemed a
new active ingredient application, subject to the registration service fee and decision
review time for a new active ingredient. In the case of a first food use application,
until that first food use is approved, any subsequent application for an additional new
food use or uses will be subject to the registration service fee and decision review
time for a first food use. Any information that (a) was neither requested nor required
by the Agency, and (b) is submitted by the applicant at the applicant’s initiative to
support the application after completion of the technical deficiency screening, and (c)
is not itself a covered registration application, must be assessed 25% of the full registration service fee for the new active ingredient or first food use application.

September 28, 2012

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FIFRA

130

TABLE 12. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW USES
Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B630

111

First food use; petition to establish a tolerance exemption (2)

13

11,577

B631

112

New food use; petition to amend
an established tolerance (3)

12

11,577

B640

113

First food use; petition to establish a tolerance (2)

19

17,365

B643
New

114

New Food use; petition to amend
tolerance exemption (3)

10

11,577

B642
New

115

First food use; indoor; food/food
handling (2)

12

28,942

B644
New

116

New use, no change to an established tolerance or tolerance exemption (3)

8

11,577

B650

117

New use; non-food (3)

7

5,789

Action

Registration
Service Fee
($)

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.

September 28, 2012

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FIFRA

Sec. 33

(2) All requests for new uses (food and/or nonfood) contained in any application for
a new active ingredient or a first food use are covered by the base fee for that new
active ingredient or first food use application and retain the same decision time review period as the new active ingredient or first food use application. The application
must be received by the agency in one package. The base fee for the category covers a
maximum of five new products. Each application for an additional new product registration and new inert approval that is submitted in the new active ingredient application package or first food use application package is subject to the registration
service fee for a new product or a new inert approval. All such associated applications
that are submitted together will be subject to the new active ingredient or first food
use decision review time. In the case of a new active ingredient application, until that
new active ingredient is approved, any subsequent application for another new product
containing the same active ingredient or an amendment to the proposed labeling will
be deemed a new active ingredient application, subject to the registration service fee
and decision review time for a new active ingredient. In the case of a first food use
application, until that first food use is approved, any subsequent application for an
additional new food use or uses will be subject to the registration service fee and decision review time for a first food use. Any information that (a) was neither requested
nor required by the Agency, and (b) is submitted by the applicant at the applicant’s
initiative to support the application after completion of the technical deficiency screening, and (c) is not itself a covered registration application, must be assessed 25% of
the full registration service fee for the new active ingredient or first food use application.
(3) Amendment applications to add the new use(s) to registered product labels are
covered by the base fee for the new use(s). All items in the covered application must
be submitted together in one package. Each application for an additional new product
registration and new inert approval(s) that is submitted in the new use application
package is subject to the registration service fee for a new product or a new inert approval. However, if a new use application only proposes to register the new use for a
new product and there are no amendments in the application, then review of one new
product application is covered by the new use fee. All such associated applications
that are submitted together will be subject to the new use decision review time. Any
application for a new product or an amendment to the proposed labeling (a) submitted
subsequent to submission of the new use application and (b) prior to conclusion of its
decision review time and (c) containing the same new uses, will be deemed a separate new-use application, subject to a separate registration service fee and new decision review time for a new use. If the new-use application includes non-food (indoor
and/or outdoor), and food (outdoor and/or indoor) uses, the appropriate fee is due for
each type of new use and the longest decision review time applies to all of the new
uses requested in the application. Any information that (a) was neither requested nor
required by the Agency, and (b) is submitted by the applicant at the applicant’s initiative to support the application after completion of the technical deficiency screen, and
(c) is not itself a covered registration application, must be assessed 25% of the full
registration service fee for the new use application.

September 28, 2012

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FIFRA

132

TABLE 13. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW PRODUCTS

EPA
No.

B652
New

September 28, 2012

New
CR
No.
118

Action

New product; registered source of
active ingredient; requires petition to amend established tolerance or tolerance exemption;
requires 1) submission of product specific data; or 2) citation
of previously reviewed and accepted data; or 3) submission
or citation of data generated at
government expense; or 4) submission or citation of scientifically-sound rationale based on
publicly available literature or
other relevant information that
addresses the data requirement; or 5) submission of a request for a data requirement to
be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply (2)

Decision
Review
Time
(Months)
(1)
13

Registration
Service Fee
($)
11,577

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FIFRA

Sec. 33

TABLE 13. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW PRODUCTS—Continued

September 28, 2012

EPA
No.

New
CR
No.

B660

119

Action

New product; registered source of
active ingredient(s); identical or
substantially similar in composition and use to a registered
product; no change in an established tolerance or tolerance
exemption. No data review, or
only product chemistry data;
cite-all data citation, or selective data citation where applicant owns all required data or
authorization from data owner
is demonstrated. Category includes 100% re-package of
registered end-use or manufacturing-use product that requires
no data submission or data
matrix. For microbial pesticides,
the active ingredient(s) must
not be re-isolated. (2)

Decision
Review
Time
(Months)
(1)
4

Registration
Service Fee
($)
1,159

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FIFRA

134

TABLE 13. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW PRODUCTS—Continued

September 28, 2012

EPA
No.

New
CR
No.

B670

120

Action

New product; registered source of
active ingredient(s); no change
in an established tolerance or
tolerance exemption; requires:
1) submission of product specific data; or 2) citation of previously reviewed and accepted
data; or 3) submission or citation of data generated at government expense; or 4) submission or citation of a scientifically-sound rationale based on
publicly available literature or
other relevant information that
addresses the data requirement; or 5) submission of a request for a data requirement to
be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. (2)

Decision
Review
Time
(Months)
(1)
7

Registration
Service Fee
($)
4,631

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FIFRA

Sec. 33

TABLE 13. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW PRODUCTS—Continued

September 28, 2012

EPA
No.

New
CR
No.

B671

121

Action

New product; unregistered source
of active ingredient(s); requires
a petition to amend an established tolerance or tolerance exemption; requires: 1) submission of product specific data;
or 2) citation of previously reviewed and accepted data; or
3) submission or citation of
data generated at government
expense; or 4) submission or
citation of a scientificallysound rationale based on publicly available literature or other
relevant information that addresses the data requirement;
or 5) submission of a request
for a data requirement to be
waived supported by a scientifically-sound rationale explaining why the data requirement
does not apply. (2)

Decision
Review
Time
(Months)
(1)
17

Registration
Service Fee
($)
11,577

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FIFRA

136

TABLE 13. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW PRODUCTS—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B672

122

New product; unregistered source
of active ingredient(s); non-food
use or food use with a tolerance or tolerance exemption
previously established for the
active ingredient(s); requires: 1)
submission of product specific
data; or 2) citation of previously reviewed and accepted
data; or 3) submission or citation of data generated at government expense; or 4) submission or citation of a scientifically-sound rationale based on
publicly available literature or
other relevant information that
addresses the data requirement; or 5) submission of a request for a data requirement to
be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. (2)

13

8,269

B673
New

123

New product MUP/EP; unregistered
source of active ingredient(s);
citation of Technical Grade Active Ingredient (TGAI) data previously reviewed and accepted
by the Agency. Requires an
Agency determination that the
cited data supports the new
product. (2)

10

4,631

Action

Registration
Service Fee
($)

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FIFRA

Sec. 33

TABLE 13. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW PRODUCTS—Continued

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

B674
New

124

New product MUP; Repack of identical registered end-use product
as a manufacturing-use product; same registered uses only
(2)

4

1,159

B675
New

125

New Product MUP; registered
source of active ingredient;
submission of completely new
generic data package; registered uses only. (2)

10

8,269

B676
New

126

New product; more than one active ingredient where one active
ingredient is an unregistered
source; product chemistry data
must be submitted; requires: 1)
submission of product specific
data, and 2) citation of previously reviewed and accepted
data; or 3) submission or citation of data generated at government expense; or 4) submission or citation of a scientifically-sound rationale based on
publicly available literature or
other relevant information that
addresses the data requirement; or 5) submission of a request for a data requirement to
be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. (2)

13

8,269

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FIFRA

138

TABLE 13. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; NEW PRODUCTS—Continued

EPA
No.

B677
New

New
CR
No.
127

Action

New end-use non-food animal
product with submission of two
or more target animal safety
studies; includes data and/or
waivers of data for only:
∑ product chemistry and/or
∑ acute toxicity and/or
∑ public health pest efficacy and/
or
∑ animal safety studies and/or
∑ child resistant packaging (2)

Decision
Review
Time
(Months)
(1)
10

Registration
Service Fee
($)
8,000

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
*ERR93*(2) An application for a new end-use product using a source of active ingredient that (a) is not yet registered but (b) has an application pending with the
Agency for review, will be considered an application for a new product with an unregistered source of active ingredient.
TABLE 14. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; AMENDMENTS

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B621

128

Amendment; Experimental Use
Permit; no change to an established temporary tolerance or
tolerance exemption.

7

4,631

B622
New

129

Amendment; Experimental Use
Permit; petition to amend an
established or temporary tolerance or tolerance exemption.

11

11,577

Action

Registration
Service Fee
($)

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FIFRA

Sec. 33

TABLE 14. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — MICROBIAL
AND BIOCHEMICAL PESTICIDES; AMENDMENTS—Continued
Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B641

130

Amendment of an established tolerance or tolerance exemption.

13

11,577

B680

131

Amendment; registered source of
active ingredient(s); no new
use(s); no changes to an established tolerance or tolerance
exemption. Requires data submission. (2)

5

4,631

B681

132

Amendment; unregistered source
of active ingredient(s). Requires
data submission. (2)

7

5,513

B683
New

133

Label amendment; requires review/
update of previous risk assessment(s) without data submission (e.g., labeling changes to
REI, PPE, PHI). (2)

6

4,631

B684
New

134

Amending non-food animal product that includes submission of
target animal safety data; previously registered (2)

8

8,000

Action

Registration
Service Fee
($)

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
*ERR93*(2) (a) EPA-initiated amendments shall not be charged registration service
fees. (b) Registrant-initiated fast-track amendments are to be completed within the
timelines specified in FIFRA Section 3(c)(3)(B) and are not subject to registration service fees. (c) Registrant-initiated fast-track amendments handled by the Antimicrobials
Division are to be completed within the timelines specified in FIFRA Section 3(h) and
are not subject to registration service fees. (d) Registrant initiated amendments submitted by notification under PR Notices, such as PR Notice 98–10, continue under PR
Notice timelines and are not subject to registration service fees. (e) Submissions with
data and requiring data review are subject to registration service fees.

September 28, 2012

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Sec. 33

FIFRA

140

TABLE 15. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — STRAIGHT
CHAIN LEPIDOPTERAN PHEROMONES(SCLPS)

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B690

135

New active ingredient; food or
non-food use. (2)

7

2,316

B700

136

Experimental Use Permit application; new active ingredient or
new use.

7

1,159

B701

137

Extend or amend Experimental Use
Permit.

4

1,159

B710

138

New product; registered source of
active ingredient(s); identical or
substantially similar in composition and use to a registered
product; no change in an established tolerance or tolerance
exemption. No data review, or
only product chemistry data;
cite-all data citation, or selective data citation where applicant owns all required data or
authorization from data owner
is demonstrated. Category includes 100% re-package of
registered end-use or manufacturing-use product that requires
no data submission or data
matrix. (3)

4

1,159

Action

Registration
Service Fee
($)

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FIFRA

Sec. 33

TABLE 15. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — STRAIGHT
CHAIN LEPIDOPTERAN PHEROMONES(SCLPS)—Continued
Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B720

139

New product; registered source of
active ingredient(s); requires: 1)
submission of product specific
data; or 2) citation of previously reviewed and accepted
data; or 3) submission or citation of data generated at government expense; or 4) submission or citation of a scientifically-sound rationale based on
publicly available literature or
other relevant information that
addresses the data requirement; or 5) submission of a request for a data requirement to
be waived supported by a scientifically-sound rationale explaining why the data requirement does not apply. (3)

5

1,159

B721

140

New product; unregistered source
of active ingredient. (3)

7

2,426

B722

141

New use and/or amendment; petition to establish a tolerance or
tolerance exemption. (4) (5)

7

2,246

B730

142

Label amendment requiring data
submission. (4)

5

1,159

Action

Registration
Service Fee
($)

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.

September 28, 2012

Q:\COMP\FIFRA\FIFRA
Sec. 33

FIFRA

142

(2) All requests for new uses (food and/or nonfood) contained in any application for
a new active ingredient or a first food use are covered by the base fee for that new
active ingredient or first food use application and retain the same decision time review period as the new active ingredient or first food use application. The application
must be received by the agency in one package. The base fee for the category covers a
maximum of five new products. Each application for an additional new product registration and new inert approval that is submitted in the new active ingredient application package or first food use application package is subject to the registration
service fee for a new product or a new inert approval. All such associated applications
that are submitted together will be subject to the new active ingredient or first food
use decision review time, except where the new inert approval decision review time is
greater than that for the new active ingredient, in which case the associated new active ingredient will be subject to the new inert approval decision review time. In the
case of a new active ingredient application, until that new active ingredient is approved, any subsequent application for another new product containing the same active ingredient or an amendment to the proposed labeling will be deemed a new active
ingredient application, subject to the registration service fee and decision review time
for a new active ingredient. In the case of a first food use application, until that first
food use is approved, any subsequent application for an additional new food use or
uses will be subject to the registration service fee and decision review time for a first
food use. Any information that (a) was neither requested nor required by the Agency,
and (b) is submitted by the applicant at the applicant’s initiative to support the application after completion of the technical deficiency screening, and (c) is not itself a
covered registration application, must be assessed 25% of the full registration service
fee for the new active ingredient or first food use application.
(3) An application for a new end-use product using a source of active ingredient
that (a) is not yet registered but (b) has an application pending with the Agency for
review, will be considered an application for a new product with an unregistered
source of active ingredient.
(4) (a) EPA-initiated amendments shall not be charged registration service fees. (b)
Registrant-initiated fast-track amendments are to be completed within the timelines
specified in FIFRA Section 3(c)(3)(B) and are not subject to registration service fees.
(c) Registrant-initiated fast-track amendments handled by the Antimicrobials Division
are to be completed within the timelines specified in FIFRA Section 3(h) and are not
subject to registration service fees. (d) Registrant initiated amendments submitted by
notification under PR Notices, such as PR Notice 98–10, continue under PR Notice
timelines and are not subject to registration service fees. (e) Submissions with data
and requiring data review are subject to registration service fees.

September 28, 2012

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(5) Amendment applications to add the new use(s) to registered product labels are
covered by the base fee for the new use(s). All items in the covered application must
be submitted together in one package. Each application for an additional new product
registration and new inert approval(s) that is submitted in the new use application
package is subject to the registration service fee for a new product or a new inert approval. However, if a new use application only proposes to register the new use for a
new product and there are no amendments in the application, then review of one new
product application is covered by the new use fee. All such associated applications
that are submitted together will be subject to the new use decision review time. Any
application for a new product or an amendment to the proposed labeling (a) submitted
subsequent to submission of the new use application and (b) prior to conclusion of its
decision review time and (c) containing the same new uses, will be deemed a separate new-use application, subject to a separate registration service fee and new decision review time for a new use. If the new-use application includes non-food (indoor
and/or outdoor), and food (outdoor and/or indoor) uses, the appropriate fee is due for
each type of new use and the longest decision review time applies to all of the new
uses requested in the application. Any information that (a) was neither requested nor
required by the Agency, and (b) is submitted by the applicant at the applicant’s initiative to support the application after completion of the technical deficiency screen, and
(c) is not itself a covered registration application, must be assessed 25% of the full
registration service fee for the new use application.
TABLE 16. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — OTHER ACT

EPA
No.

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

B614
New

143

Conditional Ruling on
Preapplication Study Waivers;
applicant-initiated

3

2,294

B615
New

144

Rebuttal of agency reviewed protocol, applicant initiated

3

2,294

B682

145

Protocol review; applicant initiated; excludes time for HSRB
review

3

2,205

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.

September 28, 2012

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FIFRA

144

TABLE 17. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — PLANT
INCORPORATED PROTECTANTS (PIPS)

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B740

146

Experimental Use Permit application; no petition for tolerance/
tolerance exemption. Includes:
1) non-food/feed use(s) for a new
(2) or registered (3) PIP;
2) food/feed use(s) for a new or
registered PIP with crop destruct;
3) food/feed use(s) for a new or
registered PIP in which an established tolerance/tolerance
exemption exists for the intended use(s). (4)

6

86,823

B750

147

Experimental Use Permit application; with a petition to establish a temporary or permanent
tolerance/tolerance exemption
for the active ingredient. Includes new food/feed use for a
registered (3) PIP. (4)

9

115,763

B770

148

Experimental Use Permit application; new (2) PIP; with petition
to establish a temporary tolerance/tolerance exemption for
the active ingredient; credit
75% of B771 fee toward registration application for a new
active ingredient that follows;
SAP review. (5)

15

173,644

Action

Registration
Service Fee
($)

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TABLE 17. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — PLANT
INCORPORATED PROTECTANTS (PIPS)—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B771

149

Experimental Use Permit application; new (2) PIP; with petition
to establish a temporary tolerance/tolerance exemption for
the active ingredient; credit
75% of B771 fee toward registration application for a new
active ingredient that follows.

10

115,763

B772

150

Application to amend or extend an
Experimental Use Permit; no
petition since the established
tolerance/tolerance exemption
for the active ingredient is unaffected.

3

11,577

B773

151

Application to amend or extend an
Experimental Use Permit; with
petition to extend a temporary
tolerance/tolerance exemption
for the active ingredient.

5

28,942

B780

152

Registration application; new (2)
PIP; non-food/feed.

12

144,704

B790

153

Registration application; new (2)
PIP; non-food/feed; SAP review.
(5)

18

202,585

B800

154

Registration application; new (2)
PIP; with petition to establish
permanent tolerance/tolerance
exemption for the active ingredient based on an existing
temporary tolerance/tolerance
exemption.

12

231,585

Action

Registration
Service Fee
($)

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FIFRA

146

TABLE 17. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — PLANT
INCORPORATED PROTECTANTS (PIPS)—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B810

155

Registration application; new (2)
PIP; with petition to establish
permanent tolerance/tolerance
exemption for the active ingredient based on an existing
temporary tolerance/tolerance
exemption. SAP review. (5)

18

289,407

B820

156

Registration application; new (2)
PIP; with petition to establish
or amend a permanent tolerance/tolerance exemption of an
active ingredient.

15

289,407

B840

157

Registration application; new (2)
PIP; with petition to establish
or amend a permanent tolerance/tolerance exemption of an
active ingredient. SAP review.
(5)

21

347,288

B851

158

Registration application; new
event of a previously registered
PIP active ingredient(s); no petition since permanent tolerance/tolerance exemption is already established for the active
ingredient(s).

9

115,763

B870

159

Registration application; registered
(3) PIP; new product; new use;
no petition since a permanent
tolerance/tolerance exemption is
already established for the active ingredient(s). (4)

9

34,729

Action

Registration
Service Fee
($)

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Sec. 33

TABLE 17. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — PLANT
INCORPORATED PROTECTANTS (PIPS)—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B880

160

Registration application; registered
(3) PIP; new product or new
terms of registration; additional
data submitted; no petition
since a permanent tolerance/
tolerance exemption is already
established for the active ingredient(s). (6) (7)

9

28,942

B881

161

Registration application; registered
(3) PIP; new product or new
terms of registration; additional
data submitted; no petition
since a permanent tolerance/
tolerance exemption is already
established for the active ingredient(s). SAP review. (5) (6)
(7)

15

86,823

B883
New

162

Registration application; new (2)
PIP, seed increase with negotiated acreage cap and timelimited registration; with petition to establish a permanent
tolerance/tolerance exemption
for the active ingredient based
on an existing temporary tolerance/tolerance exemption. (8)

9

115,763

B884
New

163

Registration application; new (2)
PIP, seed increase with negotiated acreage cap and timelimited registration; with petition to establish a permanent
tolerance/tolerance exemption
for the active ingredient. (8)

12

144,704

Action

Registration
Service Fee
($)

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Sec. 33

FIFRA

148

TABLE 17. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — PLANT
INCORPORATED PROTECTANTS (PIPS)—Continued

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

B885
New

164

Registration application; registered
(3) PIP, seed increase; breeding
stack of previously approved
PIPs, same crop; no petition
since a permanent tolerance/
tolerance exemption is already
established for the active ingredient(s). (9)

9

86,823

B890

165

Application to amend a seed increase registration; converts
registration to commercial registration; no petition since permanent tolerance/tolerance exemption is already established
for the active ingredient(s).

9

57,882

B891

166

Application to amend a seed increase registration; converts
registration to a commercial
registration; no petition since a
permanent tolerance/tolerance
exemption already established
for the active ingredient(s); SAP
review. (5)

15

115,763

B900

167

Application to amend a registration, including actions such as
extending an expiration date,
modifying an IRM plan, or adding an insect to be controlled.
(10) (11)

6

11,577

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TABLE 17. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — PLANT
INCORPORATED PROTECTANTS (PIPS)—Continued

September 28, 2012

Decision
Review
Time
(Months)
(1)

EPA
No.

New
CR
No.

B901

168

Application to amend a registration, including actions such as
extending an expiration date,
modifying an IRM plan, or adding an insect to be controlled.
SAP review. (10) (11)

12

69,458

B902

169

PIP protocol review

3

5,789

B903

170

Inert ingredient tolerance exemption; e.g., a marker such as
NPT II; reviewed in BPPD.

6

57,882

Action

Registration
Service Fee
($)

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Sec. 33

FIFRA

150

TABLE 17. — BIOPESTICIDES AND POLLUTION PREVENTION DIVISION — PLANT
INCORPORATED PROTECTANTS (PIPS)—Continued

EPA
No.

New
CR
No.

B904

171

Action

Import tolerance or tolerance exemption; processed commodities/food only (inert or active
ingredient).

Decision
Review
Time
(Months)
(1)
9

Registration
Service Fee
($)
115,763

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
*ERR93*(2) New PIP = a PIP with an active ingredient that has not been registered.
(3) Registered PIP = a PIP with an active ingredient that is currently registered.
(4) Transfer registered PIP through conventional breeding for new food/feed use,
such as from field corn to sweet corn.
(5) The scientific data involved in this category are complex. EPA often seeks technical advice from the Scientific Advisory Panel on risks that pesticides pose to wildlife,
farm workers, pesticide applicators, non-target species, as well as insect resistance,
and novel scientific issues surrounding new technologies. The scientists of the SAP
neither make nor recommend policy decisions. They provide advice on the science used
to make these decisions. Their advice is invaluable to the EPA as it strives to protect
humans and the environment from risks posed by pesticides. Due to the time it takes
to schedule and prepare for meetings with the SAP, additional time and costs are
needed.
(6) Registered PIPs stacked through conventional breeding.
(7) Deployment of a registered PIP with a different IRM plan (e.g., seed blend).
(8) The negotiated acreage cap will depend upon EPA’s determination of the potential environmental exposure, risk(s) to non-target organisms, and the risk of targeted
pest developing resistance to the pesticidal substance. The uncertainty of these risks
may reduce the allowable acreage, based upon the quantity and type of non-target organism data submitted and the lack of insect resistance management data, which is
usually not required for seed-increase registrations. Registrants are encouraged to consult with EPA prior to submission of a registration application in this category.
(9) Application can be submitted prior to or concurrently with an application for
commercial registration.
(10) For example, IRM plan modifications that are applicant-initiated.
(11) EPA-initiated amendments shall not be charged fees.

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Sec. 33

TABLE 18. — INERT INGREDIENTS, EXTERNAL REVIEW AND MISCELLANEOUS ACTIONS

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

I001

172

Approval of new food use inert ingredient (2) (3)

12

18,000

I002
New

173

Amend currently approved inert ingredient tolerance or exemption
from tolerance; new data (2)

10

5,000

I003
New

174

Amend currently approved inert ingredient tolerance or exemption
from tolerance; no new data (2)

8

3,000

I004
New

175

Approval of new non-food use
inert ingredient (2)

8

10,000

I005
New

176

Amend currently approved nonfood use inert ingredient with
new use pattern; new data (2)

8

5,000

I006
New

177

Amend currently approved nonfood use inert ingredient with
new use pattern; no new data
(2)

6

3,000

I007
New

178

Approval of substantially similar
non-food use inert ingredients
when original inert is
compositionally similar with
similar use pattern (2)

4

1,500

I008
New

179

Approval of new polymer inert ingredient, food use (2)

5

3,400

I009
New

180

Approval of new polymer inert ingredient, non food use (2)

4

2,800

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FIFRA

152

TABLE 18. — INERT INGREDIENTS, EXTERNAL REVIEW AND MISCELLANEOUS ACTIONS—
Continued

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

I010
New

181

Petition to amend a tolerance exemption descriptor to add one
or more CASRNs; no new data
(2)

6

1,500

M001
New

182

Study protocol requiring Human
Studies Review Board review as
defined in 40 CFR 26 in support of an active ingredient (4)

9

7,200

M002
New

183

Completed study requiring Human
Studies Review Board review as
defined in 40 CFR 26 in support of an active ingredient (4)

9

7,200

M003
New

184

External technical peer review of
new active ingredient, product,
or amendment (e.g., consultation with FIFRA Scientific Advisory Panel) for an action with a
decision timeframe of less than
12 months. Applicant initiated
request based on a requirement
of the Administrator, as defined
by FIFRA § 25(d), in support of
a novel active ingredient, or
unique use pattern or application technology. Excludes PIP
active ingredients. (5)

12

58,000

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TABLE 18. — INERT INGREDIENTS, EXTERNAL REVIEW AND MISCELLANEOUS ACTIONS—
Continued

EPA
No.

September 28, 2012

New
CR
No.

Action

Decision
Review
Time
(Months)
(1)

Registration
Service Fee
($)

M004
New

185

External technical peer review of
new active ingredient, product,
or amendment (e.g., consultation with FIFRA Scientific Advisory Panel) for an action with a
decision timeframe of greater
than 12 months. Applicant initiated request based on a requirement of the Administrator,
as defined by FIFRA § 25(d), in
support of a novel active ingredient, or unique use pattern or
application technology. Excludes
PIP active ingredients. (5)

18

58,000

M005
New

186

New Product: Combination, Contains a combination of active
ingredients from a registered
and/or unregistered source;
conventional, antimicrobial and/
or biopesticide. Requires coordination with other regulatory divisions to conduct review of
data, label and/or verify the
validity of existing data as
cited. Only existing uses for
each active ingredient in the
combination product. (6) (7)

9

20,000

M006
New

187

Request for up to 5 letters of certification (Gold Seal) for one
actively registered product.

1

250

M007
New

188

Request to extend Exclusive Use of
data as provided by FIFRA Section 3(c)(1)(F)(ii)

12

5,000

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FIFRA

154

TABLE 18. — INERT INGREDIENTS, EXTERNAL REVIEW AND MISCELLANEOUS ACTIONS—
Continued

EPA
No.

M008
New

New
CR
No.
189

Action

Request to grant Exclusive Use of
data as provided by FIFRA Section 3(c)(1)(F)(vi) for a minor
use, when a FIFRA Section
2(ll)(2) determination is required

Decision
Review
Time
(Months)
(1)
10

Registration
Service Fee
($)
1,500

(1) A decision review time that would otherwise end on a Saturday, Sunday, or federal holiday, will be extended to end on the next business day.
(2) If another covered application is associated with and dependent upon a pending
application for an inert ingredient action, each application will be subject to its respective registration service fee. The decision review time for the other associated covered application will be extended to match the PRIA due date of the pending inert ingredient action, unless the PRIA due date for the other associated covered action is
further out, in which case it will be subject to its own decision review time. If the application covers multiple ingredients grouped by EPA into one chemical class, a single
registration service fee will be assessed for approval of those ingredients.
(3) If EPA data rules are amended to newly require clearance under section 408 of
the FFDCA for an ingredient of an antimicrobial product where such ingredient was not
previously subject to such a clearance, then review of the data for such clearance of
such product is not subject to a registration service fee for the tolerance action for
two years from the effective date of the rule.
(4) Any other covered application that is associated with and dependent on the
HSRB review will be subject to its separate registration service fee. The decision review times for the associated actions run concurrently, but will end at the date of the
latest review time.
(5) Any other covered application that is associated with and dependent on the SAP
review will be subject to its separate registration service fee. The decision review time
for the associated action will be extended by the decision review time for the SAP review.
(6) An application for a new end-use product using a source of active ingredient
that (a) is not yet registered but (b) has an application pending with the Agency for
review, will be considered an application for a new product with an unregistered
source of active ingredient.

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Sec. 33

(7) Where the action involves approval of a new or amended label, on or before the
end date of the decision review time, the Agency shall provide to the applicant a draft
accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it
be issued as the accepted final Agency-stamped label; or (b) does not agree to one or
more of the terms of the draft accepted label as amended by the Agency and requests
additional time to resolve the difference(s); or (c) withdraws the application without
prejudice for subsequent resubmission, but forfeits the associated registration service
fee. For cases described in (b), the applicant shall have up to 30 calendar days to
reach agreement with the Agency on the final terms of the Agency-accepted label. If
the applicant agrees to all of the terms of the accepted label as in (a), including upon
resolution of differences in (b), the Agency shall provide an accepted final Agencystamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency.
(4) PENDING PESTICIDE REGISTRATION APPLICATIONS.—
(A) IN GENERAL.—An applicant that submitted a registration application to the Administrator before the effective date of the Pesticide Registration Improvement Act of
2003, but that is not required to pay a registration service
fee under paragraph (2)(B), may, on a voluntary basis, pay
a registration service fee in accordance with paragraph
(2)(B).
(B) VOLUNTARY FEE.—The Administrator may not
compel payment of a registration service fee for an application described in subparagraph (A).
(C) DOCUMENTATION.—An application for which a voluntary registration service fee is paid under this paragraph shall be submitted with documentation certifying—
(i) payment of the registration service fee; or
(ii) a request for a waiver from or reduction of the
registration service fee.
(5) RESUBMISSION OF PESTICIDE REGISTRATION APPLICATIONS.—If a pesticide registration application is submitted by
a person that paid the fee for the application under paragraph
(2), is determined by the Administrator to be complete, and is
not approved or is withdrawn (without a waiver or refund), the
submission of the same pesticide registration application by
the same person (or a licensee, assignee, or successor of the
person) shall not be subject to a fee under paragraph (2).
(6) FEE ADJUSTMENT.—
(A) IN GENERAL.—Effective for a covered pesticide registration application received during the period beginning
on October 1, 2013, and ending on September 30, 2015, the
Administrator shall increase by 5 percent the registration
service fee payable for the application under paragraph (3).
(B) ADDITIONAL ADJUSTMENT.—Effective for a covered
pesticide registration application received on or after October 1, 2015, the Administrator shall increase by an additional 5 percent the registration service fee in effect as of
September 30, 2015.
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156

(C) PUBLICATION.—The Administrator shall publish in
the Federal Register the revised registration service fee
schedules.
(7) WAIVERS AND REDUCTIONS.—
(A) IN GENERAL.—An applicant for a covered pesticide
registration may request the Administrator to waive or reduce the amount of a registration service fee payable
under this section under the circumstances described in
subparagraphs (D) through (G).
(B) DOCUMENTATION.—
(i) IN GENERAL.—A request for a waiver from or
reduction of the registration service fee shall be accompanied by appropriate documentation demonstrating the basis for the waiver or reduction.
(ii) CERTIFICATION.—The applicant shall provide
to the Administrator a written certification, signed by
a responsible officer, that the documentation submitted to support the waiver or reduction request is
accurate.
(iii) INACCURATE DOCUMENTATION.—An application
shall be subject to the applicable registration service
fee payable under paragraph (3) if, at any time, the
Administrator determines that—
(I) the documentation supporting the waiver
or reduction request is not accurate; or
(II) based on the documentation or any other
information, the waiver or reduction should not
have been granted or should not be granted.
(C) DETERMINATION TO GRANT OR DENY REQUEST.—As
soon as practicable, but not later than 60 days, after the
date on which the Administrator receives a request for a
waiver or reduction of a registration service fee under this
paragraph, the Administrator shall—
(i) determine whether to grant or deny the request; and
(ii) notify the applicant of the determination.
(D) MINOR USES.—
(i) IN GENERAL.—The Administrator may exempt
from, or waive a portion of, the registration service fee
for an application for minor uses for a pesticide.
(ii) SUPPORTING DOCUMENTATION.—An applicant
requesting a waiver or exemption under this subparagraph shall provide supporting documentation that
demonstrates, to the satisfaction of the Administrator,
that anticipated revenues from the uses that are the
subject of the application would be insufficient to justify imposition of the full application fee.
(E) IR–4 EXEMPTION.—The Administrator shall exempt
an application from the registration service fee if the Administrator determines that—
(i) the application is solely associated with a tolerance petition submitted in connection with the InterRegional Project Number 4 (IR–4) as described in section 2 of Public Law 89–106 (7 U.S.C. 450i(e)); and
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Sec. 33

(ii) the exemption is in the public interest.
(F) SMALL BUSINESSES.—
(i) IN GENERAL.—The Administrator shall waive
50 percent of the registration service fees payable by
an entity for a covered pesticide registration application under this section if the entity is a small business
(as defined in section 4(i)(1)(E)(ii)) at the time of application.
(ii) WAIVER OF FEES.—The Administrator shall
waive 75 percent of the registration service fees payable by an entity under this section if the entity—
(I) is a small business (as defined in section
4(i)(1)(E)(ii)) at the time of application; and
(II) has average annual global gross revenues
described in section 4(i)(1)(E)(ii)(I)(bb) that does
not exceed $10,000,000, at the time of application.
(iii) FORMATION FOR WAIVER.—The Administrator
shall not grant a waiver under this subparagraph if
the Administrator determines that the entity submitting the application has been formed or manipulated
primarily for the purpose of qualifying for the waiver.
(iv) DOCUMENTATION.—An entity requesting a
waiver under this subparagraph shall provide to the
Administrator—
(I) documentation demonstrating that the entity is a small business (as defined in section
4(i)(1)(E)(ii)) at the time of application; and
(II) if the entity is requesting a waiver of 75
percent of the applicable registration service fees
payable under this section, documentation demonstrating that the entity has an average annual
global gross revenue described in section
4(i)(1)(E)(ii)(I)(bb)
that
does
not
exceed
$10,000,000, at the time of application.
(G) FEDERAL AND STATE AGENCY EXEMPTIONS.—An
agency of the Federal Government or a State government
shall be exempt from covered registration service fees
under this section.
(8) REFUNDS.—
(A) EARLY WITHDRAWALS.—If, during the first 60 days
after the beginning of the applicable decision time review
period under subsection (f)(3), a covered pesticide registration application is withdrawn by the applicant, the Administrator shall refund all but 25 percent of the total registration service fee payable under paragraph (3) for the
application.
(B) WITHDRAWALS AFTER THE FIRST 60 DAYS OF DECISION REVIEW TIME PERIOD.—
(i) IN GENERAL.—If a covered pesticide registration
application is withdrawn after the first 60 days of the
applicable decision time review period, the Administrator shall determine what portion, if any, of the total
registration service fee payable under paragraph (3)
for the application may be refunded based on the proSeptember 28, 2012

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portion of the work completed at the time of withdrawal.
(ii) TIMING.—The Administrator shall—
(I) make the determination described in
clause (i) not later than 90 days after the date the
application is withdrawn; and
(II) provide any refund as soon as practicable
after the determination.
(C) DISCRETIONARY REFUNDS.—
(i) IN GENERAL.—In the case of a pesticide registration application that has been filed with the Administrator and has not been withdrawn by the applicant, but for which the Administrator has not yet
made a final determination, the Administrator may refund a portion of a covered registration service fee if
the Administrator determines that the refund is justified.
(ii) BASIS.—The Administrator may provide a refund for an application under this subparagraph—
(I) on the basis that, in reviewing the application, the Administrator has considered data submitted in support of another pesticide registration
application;
(II) on the basis that the Administrator completed portions of the review of the application before the effective date of this section; or
(III) on the basis that the Administrator rejected the application under subsection (f)(4)(B).
(D) CREDITED FEES.—In determining whether to grant
a refund under this paragraph, the Administrator shall
take into account any portion of the registration service
fees credited under paragraph (2) or (4).
(c) PESTICIDE REGISTRATION FUND.—
(1) ESTABLISHMENT.—There is established in the Treasury
of the United States a Pesticide Registration Fund to be used
in carrying out this section (referred to in this section as the
‘‘Fund’’), consisting of—
(A) such amounts as are deposited in the Fund under
paragraph (2);
(B) any interest earned on investment of amounts in
the Fund under paragraph (5); and
(C) any proceeds from the sale or redemption of investments held in the Fund.
(2) DEPOSITS IN FUND.—Subject to paragraph (4), the Administrator shall deposit fees collected under this section in the
Fund.
(3) EXPENDITURES FROM FUND.—
(A) IN GENERAL.—Subject to subparagraphs (B) and
(C) and paragraph (4), the Administrator may make expenditures from the Fund—
(i) to cover the costs associated with the review
and decisionmaking pertaining to all applications for
which registration service fees have been paid under
this section; and
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(ii) to otherwise carry out this section.
(B) WORKER PROTECTION.—
(i) IN GENERAL.—For each of fiscal years 2013
through 2017, the Administrator shall use approximately 1⁄17 of the amount in the Fund (but not less
than $1,000,000) to enhance scientific and regulatory
activities relating to worker protection.
(ii) PARTNERSHIP GRANTS.—Of the amounts in the
Fund, the Administrator shall use for partnership
grants, for each of fiscal years 2013 through 2017,
$500,000.
(iii) PESTICIDE SAFETY EDUCATION PROGRAM.—Of
the amounts in the Fund, the Administrator shall use
$500,000 for each of fiscal years 2013 through 2017 to
carry out the pesticide safety education program.
(4) COLLECTIONS AND APPROPRIATIONS ACTS.—The fees authorized by this section and amounts deposited in the Fund—
(A) shall be collected and made available for obligation
only to the extent provided in advance in appropriations
Acts; and
(B) shall be available without fiscal year limitation.
(5) UNUSED FUNDS.—
(A) IN GENERAL.—Amounts in the Fund not currently
needed to carry out this section shall be—
(i) 33–2 maintained readily available or on deposit;
(ii) invested in obligations of the United States or
guaranteed by the United States; or
(iii) invested in obligations, participations, or other instruments that are lawful investments for fiduciary, trust,
or public funds.
(B) USE OF INVESTMENT INCOME.—After consultation
with the Secretary of the Treasury, the Administrator may
use income from investments described in clauses (ii) and
(iii) of subparagraph (A) to carry out this section.
(d) ASSESSMENT OF FEES.—
(1) DEFINITION OF COVERED FUNCTIONS.—In this subsection, the term ‘‘covered functions’’ means functions of the
Office of Pesticide Programs of the Environmental Protection
Agency, as identified in key programs and projects of the final
operating plan for the Environmental Protection Agency submitted as part of the budget process for fiscal year 2002, regardless of any subsequent transfer of 1 or more of the functions to another office or agency or the subsequent transfer of
a new function to the Office of Pesticide Programs.
(2) MINIMUM AMOUNT OF APPROPRIATIONS.—Registration
service fees may not be assessed for a fiscal year under this
section unless the amount of appropriations for salaries, contracts, and expenses for the functions (as in existence in fiscal
year 2012) of the Office of Pesticide Programs of the Environmental Protection Agency for the fiscal year (excluding the
amount of any fees appropriated for the fiscal year) are equal
33–2 Indentation of clauses (i) through (iii) is so in original (as amended by sec. 5(e)(3)(A) of
Public Law 110–94). Clauses probably should be indented.

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to or greater than the amount of appropriations for covered
functions for fiscal year 2012 (excluding the amount of any fees
appropriated for the fiscal year).
(3) USE OF FEES.—Registration service fees authorized by
this section shall be available, in the aggregate, only to defray
increases in the costs associated with the review and decisionmaking for the review of pesticide registration applications and
associated tolerances (including increases in the number of
full-time equivalent positions in the Environmental Protection
Agency engaged in those activities) over the costs for fiscal
year 2002, excluding costs paid from fees appropriated for the
fiscal year.
(4) SUBSEQUENT AUTHORITY.—If the Administrator does
not assess registration service fees under subsection (b) during
any portion of a fiscal year as the result of paragraph (2) and
is subsequently permitted to assess the fees under subsection
(b) during the fiscal year, the Administrator shall assess and
collect the fees, without any modification in rate, at any time
during the fiscal year, notwithstanding any provisions of subsection (b) relating to the date fees are to be paid.
(e) REFORMS TO REDUCE DECISION TIME REVIEW PERIODS.—To
the maximum extent practicable consistent with the degrees of risk
presented by pesticides and the type of review appropriate to evaluate risks, the Administrator shall identify and evaluate reforms to
the pesticide registration process under this Act with the goal of reducing decision review periods in effect on the effective date of the
Pesticide Registration Improvement Extension Act of 2012 for pesticide registration actions for covered pesticide registration applications (including reduced risk applications).
(f) DECISION TIME REVIEW PERIODS.—
(1) IN GENERAL.—Not later than 30 days after the effective
date of the Pesticide Registration Improvement Extension Act
of 2012, the Administrator shall make publicly available a
schedule of decision review periods for covered pesticide registration actions and corresponding registration service fees
under this Act.
(2) REPORT.—The schedule shall be the same as the applicable schedule provided under subsection (b)(3).
(3) APPLICATIONS SUBJECT TO DECISION TIME REVIEW PERIODS.—The decision time review periods specified in paragraph
(1) shall apply to—
(A) covered pesticide registration applications subject
to registration service fees under subsection (b)(2);
(B) covered pesticide registration applications for
which an applicant has voluntarily paid registration service fees under subsection (b)(4); and
(C) covered pesticide registration applications listed in
the Registration Division 2003 Work Plan of the Office of
Pesticide Programs of the Environmental Protection Agency.
(4) START OF DECISION TIME REVIEW PERIOD.—
(A) IN GENERAL.—Except as provided in subparagraphs (C), (D), and (E), in the case of a pesticide registration application accompanied by the registration service
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fee required under this section, the decision time review
period begins 21 days after the date on which the Administrator receives the covered pesticide registration application and fee.
(B) INITIAL CONTENT AND PRELIMINARY TECHNICAL
SCREENINGS.—
(i) SCREENINGS.—
(I) INITIAL CONTENT.—Not later than 21 days
after receiving an application and the required
registration service fee, the Administrator shall
conduct an initial screening of the contents of the
application in accordance with clause (iii).
(II) PRELIMINARY TECHNICAL SCREENING.—
After conducting the initial content screening described in subclause (I) and in accordance with
clause (iv), the Administrator shall conduct a preliminary technical screening—
(aa) not later than 45 days after the date
on which the decision time review period begins (for applications with decision time review periods of not more than 180 days); and
(bb) not later than 90 days after the date
on which the decision time review period begins (for applications with decision time review periods greater than 180 days).
(ii) REJECTION.—
(I) IN GENERAL.—If the Administrator determines at any time before the Administrator completes the preliminary technical screening under
clause (i)(II) that the application failed the initial
content or preliminary technical screening and the
applicant does not correct the failure before the
date that is 10 business days after the applicant
receives a notification of the failure, the Administrator shall reject the application.
(II) WRITTEN NOTIFICATION.—The Administrator shall make every effort to provide a written
notification of a rejection under subclause (I) during the 10-day period that begins on the date the
Administrator completes the preliminary technical
screening.
(iii) REQUIREMENTS OF INITIAL CONTENT SCREENING.—In conducting an initial content screening of an
application, the Administrator shall determine whether—
(I)(aa) the applicable registration service fee
has been paid; or
(bb) at least 25 percent of the applicable registration service fee has been paid and the application contains a waiver or refund request for the
outstanding amount and documentation establishing the basis for the waiver request; and
(II) the application appears to contain all the
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matted in accordance with guidance published by
the Administrator.
(iv) REQUIREMENTS OF PRELIMINARY TECHNICAL
SCREENING.—In conducting a preliminary technical
screening of an application, the Administrator shall
determine if—
(I) the application and the data and information submitted with the application are accurate
and complete; and
(II) the application, data, and information are
consistent with the proposed labeling and any proposal for a tolerance or exemption from the requirement for a tolerance under section 408 of the
Federal Food, Drug, and Cosmetic Act (21 U.S.C.
346a), and are such that, subject to full review
under the standards of this Act, could result in
the granting of the application.
(C) APPLICATIONS WITH WAIVER OR REDUCTION REQUESTS.—
(i) IN GENERAL.—In the case of an application submitted with a request for a waiver or reduction of registration service fees under subsection (b)(7), the decision time review period shall be determined in accordance with this subparagraph.
(ii) REQUEST GRANTED WITH NO ADDITIONAL FEES
REQUIRED.—If the Administrator grants the waiver or
reduction request and no additional fee is required,
the decision time review period begins on the earlier
of—
(I) the date on which the Administrator
grants the request; or
(II) the date that is 60 days after the date of
receipt of the application.
(iii) REQUEST GRANTED WITH ADDITIONAL FEES REQUIRED.—If the Administrator grants the waiver or reduction request, in whole or in part, but an additional
registration service fee is required, the decision time
review period begins on the date on which the Administrator receives certification of payment of the applicable registration service fee.
(iv) REQUEST DENIED.—If the Administrator denies the waiver or reduction request, the decision time
review period begins on the date on which the Administrator receives certification of payment of the applicable registration service fee.
(D) PENDING APPLICATIONS.—
(i) IN GENERAL.—The start of the decision time review period for applications described in clause (ii)
shall be the date on which the Administrator receives
certification of payment of the applicable registration
service fee.
(ii) APPLICATIONS.—Clause (i) applies to—
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(I) covered pesticide registration applications
for which voluntary fees have been paid under
subsection (b)(4); and
(II) covered pesticide registration applications
received on or after the effective date of the Pesticide Registration Improvement Act of 2003 but
submitted without the applicable registration
service fee required under this section due to the
inability of the Administrator to assess fees under
subsection (d)(1).
(E) 2003 WORK PLAN.—In the case of a covered pesticide registration application listed in the Registration Division 2003 Work Plan of the Office of Pesticide Programs
of the Environmental Protection Agency, the decision time
review period begins on the date that is 30 days after the
effective date of the Pesticide Registration Improvement
Act of 2003.
(5) EXTENSION OF DECISION TIME REVIEW PERIOD.—The Administrator and the applicant may mutually agree in writing
to extend a decision time review period under this subsection.
(g) JUDICIAL REVIEW.—
(1) IN GENERAL.—Any applicant adversely affected by the
failure of the Administrator to make a determination on the
application of the applicant for registration of a new active ingredient or new use for which a registration service fee is paid
under this section may obtain judicial review of the failure
solely under this section.
(2) SCOPE.—
(A) IN GENERAL.—In an action brought under this subsection, the only issue on review is whether the Administrator failed to make a determination on the application
specified in paragraph (1) by the end of the applicable decision time review period required under subsection (f) for
the application.
(B) OTHER ACTIONS.—No other action authorized or required under this section shall be judicially reviewable by
a Federal or State court.
(3) TIMING.—
(A) IN GENERAL.—A person may not obtain judicial review of the failure of the Administrator to make a determination on the application specified in paragraph (1) before the expiration of the 2-year period that begins on the
date on which the decision time review period for the application ends.
(B) MEETING WITH ADMINISTRATOR.—To be eligible to
seek judicial review under this subsection, a person seeking the review shall first request in writing, at least 120
days before filing the complaint for judicial review, a decision review meeting with the Administrator.
(4) REMEDIES.—The Administrator may not be required or
permitted to refund any portion of a registration service fee
paid in response to a complaint that the Administrator has
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istration application specified in paragraph (1) by the end of
the applicable decision review period.
(h) ACCOUNTING.—The Administrator shall—
(1) provide an annual accounting of the registration service
fees paid to the Administrator and disbursed from the Fund,
by providing financial statements in accordance with—
(A) the Chief Financial Officers Act of 1990 (Public
Law 101–576; 104 Stat. 2838) and amendments made by
that Act; and
(B) the Government Management Reform Act of 1994
(Public Law 103–356; 108 Stat. 3410) and amendments
made by that Act;
(2) provide an accounting describing expenditures from the
Fund authorized under subsection (c); and
(3) provide an annual accounting describing collections and
expenditures authorized under subsection (d).
(i) AUDITING.—
(1) FINANCIAL STATEMENTS OF AGENCIES.—For the purpose
of section 3515(c) of title 31, United States Code, the Fund
shall be considered a component of an executive agency.
(2) COMPONENTS.—The annual audit required under sections 3515(b) and 3521 of that title of the financial statements
of activities under this section shall include an analysis of—
(A) the fees collected under subsection (b) and disbursed;
(B) compliance with subsection (f);
(C) the amount appropriated to meet the requirements
of subsection (d)(1); and
(D) the reasonableness of the allocation of the overhead allocation of costs associated with the review and decisionmaking pertaining to applications under this section.
(3) INSPECTOR GENERAL.—The Inspector General of the Environmental Protection Agency shall—
(A) conduct the annual audit required under this subsection; and
(B) report the findings and recommendations of the
audit to the Administrator and to the appropriate committees of Congress.
(j) PERSONNEL LEVELS.—All full-time equivalent positions supported by fees authorized and collected under this section shall not
be counted against the agency-wide personnel level goals of the Environmental Protection Agency.
(k) REPORTS.—
(1) IN GENERAL.—Not later than March 1, 2005, and each
March 1 thereafter through March 1, 2017, the Administrator
shall publish an annual report describing actions taken under
this section.
(2) CONTENTS.—The report shall include—
(A) a review of the progress made in carrying out each
requirement of subsections (e) and (f), including—
(i) the number of applications reviewed, including
the decision times for each application specified in
subsection (f);
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(ii) the number of label amendments that have
been reviewed using electronic means;
(iii) the amount of money from the Reregistration
and Expedited Processing Fund used to carry out inert
ingredient review and review of similar applications
under section 4(k)(3);
(iv) the number of applications completed for identical or substantially similar applications under section 3(c)(3)(B), including the number of such applications completed within 90 days pursuant to that section;
(v) the number of actions pending in each category
of actions described in subsection (f)(3), as well as the
number of inert ingredients;
(vi) to the extent determined appropriate by the
Administrator and consistent with the authorities of
the Administrator and limitations on delegation of
functions by the Administrator, recommendations
for—
(I) expanding the use of self-certification in all
appropriate areas of the registration process;
(II) providing for accreditation of outside reviewers and the use of outside reviewers to conduct the review of major portions of applications;
(III) reviewing the scope of use of the notification process to cover broader categories of registration actions;
(IV) providing for electronic submission and
review of labels, including process improvements
to further enhance the procedures used in electronic label review; and
(V) the allowance and use of summaries of
acute toxicity studies;
(vii) the use of performance-based contracts, other
contracts, and procurement to ensure that—
(I) the goals of this Act for the timely review
of applications for registration are met; and
(II) the registration program is administered
in the most productive and cost effective manner
practicable; and
(viii) the number of extensions of decision time review periods agreed to under subsection (f)(5) along
with a description of the reason that the Administrator was unable to make a decision within the initial
decision time review period;
(B) a description of the staffing and resources relating
to the costs associated with the review and decisionmaking
pertaining to applications;
(C) a review of the progress in meeting the timeline
requirements of section 4(g);
(D) a review of the progress in carrying out section
3(g), including—
(i) the number of pesticides or pesticide cases reviewed;
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(ii) a description of the staffing and resources relating to the costs associated with the review and decision making relating to reregistration and registration
review for compliance with the deadlines specified in
this Act;
(iii) to the extent determined appropriate by the
Administrator and consistent with the authorities of
the Administrator and limitations on delegation of
functions by the Administrator, recommendations
for—
(I) process improvements in the handling of
registration review under section 3(g);
(II) providing for accreditation of outside reviewers and the use of outside reviewers in the
registration review process; and
(III) streamlining the registration review
process, consistent with section 3(g);
(E) a review of the progress in meeting the timeline
requirements for the review of antimicrobial pesticide
products under section 3(h);
(F) a review of the progress in carrying out the review
of inert ingredients, including the number of applications
pending, the number of new applications, the number of
applications reviewed, staffing, and resources devoted to
the review of inert ingredients and recommendations to
improve the timeliness of review of inert ingredients;
(G) a review of the progress made toward—
(i) carrying out section 4(k)(4) and the amounts
from the Reregistration and Expedited Processing
Fund used for the purposes described in that section;
(ii) implementing systems for the electronic tracking of registration submissions by December 31, 2013;
(iii) implementing a system for tracking the status
of conditional registrations, including making nonconfidential information related to the conditional registrations publicly available by December 31, 2013;
(iv) implementing enhancements to the endangered species knowledge database, including making
nonconfidential information related to the database
publicly available;
(v) implementing the capability to electronically
submit and review labels submitted with registration
actions;
(vi) acquiring and implementing the capability to
electronically assess and evaluate confidential statements of formula submitted with registration actions
by December 31, 2014; and
(vii) facilitating public participation in certain registration actions and the registration review process
by providing electronic notification to interested parties of additions to the public docket;
(H) the number of applications rejected by the Administrator under the initial content and preliminary technical
screening conducted under subsection (f)(4);
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(I) a review of the progress made in updating the Pesticide Incident Data System, including progress toward
making the information contained in the System available
to the public (as the Administrator determines is appropriate); and
(J) an assessment of the public availability of summary pesticide usage data.
(3) METHOD.—The Administrator shall publish a report required by this subsection by such method as the Administrator
determines to be the most effective for efficiently disseminating
the report, including publication of the report on the Internet
site of the Environmental Protection Agency.
(4) OTHER REPORT.—
(A) SCOPE.—In addition to the annual report described
in paragraph (1), not later than October 1, 2016, the Administrator shall submit to the Committee on Agriculture
of the House of Representatives and the Committee on Agriculture, Nutrition, and Forestry of the Senate a report
that includes an analysis of the impact of maintenance
fees on small businesses that have—
(i) 10 or fewer employees; and
(ii) annual global gross revenue that does not exceed $2,000,000.
(B) INFORMATION REQUIRED.—In conducting the analysis described in subparagraph (A), the Administrator
shall collect, and include in the report under that subparagraph, information on—
(i) the number of small businesses described in
subparagraph (A) that are paying maintenance fees;
and
(ii) the number of registrations each company
holds.
(l) SAVINGS CLAUSE.—Nothing in this section affects any other
duties, obligations, or authorities established by any other section
of this Act, including the right to judicial review of duties, obligations, or authorities established by any other section of this Act.
(m) TERMINATION OF EFFECTIVENESS.—
(1) IN GENERAL.—Except as provided in paragraph (2), the
authority provided by this section terminates on September 30,
2017.
(2) PHASE OUT.—
(A) FISCAL YEAR 2018.—During fiscal year 2018, the requirement to pay and collect registration service fees applies, except that the level of registration service fees payable under this section shall be reduced 40 percent below
the level in effect on September 30, 2017.
(B) FISCAL YEAR 2019.—During fiscal year 2019, the requirement to pay and collect registration service fees applies, except that the level of registration service fees payable under this section shall be reduced 70 percent below
the level in effect on September 30, 2017.
(C) SEPTEMBER 30, 2019.—Effective September 30,
2019, the requirement to pay and collect registration service fees terminates.
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(D) DECISION REVIEW PERIODS.—
(i) PENDING APPLICATIONS.—In the case of an application received under this section before September
30, 2017, the application shall be reviewed in accordance with subsection (f).
(ii) NEW APPLICATIONS.—In the case of an application received under this section on or after September
30, 2017, subsection (f) shall not apply to the application.
SEC. 34. ø7 U.S.C. 136x¿ SEVERABILITY.

If any provision of this Act or the application thereof to any
person or circumstance is held invalid, the invalidity shall not affect other provisions or applications of this Act which can be given
effect without regard to the invalid provision or application, and to
this end the provisions of this Act are severable.
SEC. 35. ø7 U.S.C. 136y¿ AUTHORIZATION FOR APPROPRIATIONS.

There is authorized to be appropriated to carry out this Act
(other than section 23(a))—
(1) $83,000,000 for fiscal year 1989, of which not more
than $13,735,500 shall be available for research under this
Act;
(2) $95,000,000 for fiscal year 1990, of which not more
than $14,343,600 shall be available for research under this
Act; and
(3) $95,000,000 for fiscal year 1991, of which not more
than $14,978,200 shall be available for research under this
Act.

September 28, 2012