Submission of Unreasonable Adverse Effects Information Under FIFRA Section 6(a)(2)

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
1204.11_attach_-_F.doc	Supplementary Document	Uploaded 2010-08-10	Available
attach- G Consultation Questions and Responses 6a2.doc	Supplementary Document	Uploaded 2010-07-02	Available
attach - H.doc	Supplementary Document	Uploaded 2010-07-02	Available
1204attach-E.pdf	Supplementary Document	Uploaded 2010-07-02	Available
1204attach-D.pdf	Supplementary Document	Uploaded 2010-07-02	Available
1204attach-C.pdf	Supplementary Document	Uploaded 2010-07-02	Available
1204attach-B.pdf	Supplementary Document	Uploaded 2010-07-02	Available
1204attach-A.pdf	Supplementary Document	Uploaded 2010-07-02	Available
1204ss11.doc	Supporting Statement A	Uploaded 2010-08-26	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
24885	FIFRA Section 6(a)(2) Submisssions - Studies		Modified
194496	FIFRA Section 6(a)(2) - Training		New
194495	FIFRA Section 6(a)(2) Submissions - Incidents		New

ICR Details

OMB Control No: 2070-0039	ICR Reference No: 201009-2070-001
Status: Historical Active	Previous ICR Reference No: 200704-2070-002
Agency/Subagency: EPA/OCSPP	Agency Tracking No: 1204.11
Title: Submission of Unreasonable Adverse Effects Information Under FIFRA Section 6(a)(2)
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 09/30/2011
	Date Received in OIRA: 09/07/2010
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/2014	36 Months From Approved	09/30/2011
Responses	91,979	0	54,240
Time Burden (Hours)	203,236	0	167,316
Cost Burden (Dollars)	0	0	0

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Abstract: This is a renewal of an existing ICR that is currently approved by OMB and is due to expire October 31, 2010. Section 6(a)(2) of the Federal Insecticide, Fungicide and Rodenticide Act (FIFRA) requires pesticide registrants to submit information to the Agency which may be relevant to the balancing of the risks and benefits of a pesticide product. The statute requires the registrant to submit any factual information that it acquires regarding adverse effects associated with its pesticidal products, and it is up to the Agency to determine whether or not that factual information constitutes an unreasonable adverse effect. In order to limit the amount of less meaningful information that might be submitted to the Agency, the EPA has limited the scope of factual information that the registrant must submit. The agency?s regulations at 40 CFR 159 provide a detailed description of the reporting obligations of registrants under FIFRA section 6(a)(2). Potential respondents affected by the collection activities under this ICR include anyone who holds or ever held a registration for a pesticide product issued under FIFRA section 3 or 24(c). The North American Industrial Classification System (NAICS) code is 325320 (Pesticide and Other Agricultural Chemical Manufacturing).

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Authorizing Statute(s): US Code: 7 USC 136d(a)(2) Name of Law: Section 6(a)(2) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA)
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	75 FR 8336	02/24/2010
30-day Notice:	Federal Register Citation:	Citation Date:
	75 FR 54338	09/07/2010
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 3

table that charts list of burden

IC Title	Form No.	Form Name
FIFRA Section 6(a)(2) Submissions - Incidents
FIFRA Section 6(a)(2) Submisssions - Studies
FIFRA Section 6(a)(2) - Training

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ICR Summary of Burden

table that charts list of burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	91,979	54,240	0	0	37,739	0
Annual Time Burden (Hours)	203,236	167,316	0	0	35,920	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $1,064,533

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 09/07/2010

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