OMB files this
comment in accordance with 5 CFR 1320.11( c ). This OMB action is
not an approval to conduct or sponsor an information collection
under the Paperwork Reduction Act of 1995. This action has no
effect on any current approvals. If OMB has assigned this ICR a new
OMB Control Number, the OMB Control Number will not appear in the
active inventory. For future submissions of this information
collection, reference the OMB Control Number provided.
Inventory as of this Action
Requested
Previously Approved
09/30/2022
36 Months From Approved
09/30/2022
51,825
0
51,825
1,778,244
0
1,778,244
8,285,600
0
8,285,600
CAA section 112(r)(7) required EPA to
promulgate regulations and appropriate guidance to provide for the
prevention and detection of accidental releases and for responses
to such releases. EPA issued the final rule on June 20, 1996 (61 FR
31668). The regulations include requirements for submittal of an
RMP, including source registration, to EPA. The RMP includes
information on a sources hazard assessment, prevention program, and
emergency response program. The regulations are codified in 40 CFR
part 68. The rule requires sources to submit their RMPs every five
years beginning June 21, 1999. The final rule establishing the list
of regulated substances and threshold quantities under CAA section
112r was published on January 31, 1994 (59 FR 4478), which also
includes provisions and procedures for submitting a petition to add
or delete a substance. The information collection request (ICR)
(EPA ICR No. 1656.15, OMB Control No. 2050-0144) addressed the
following information requirements: (1) Documenting sources risk
management programs and submitting a source risk management plan
(RMP) under CAA Section 112(r)(7). The regulations include
requirements for covered sources to implement and maintain
documentation for a risk management program and submit a RMP
(including information on a sources hazard assessment, prevention
program, and emergency response program) to EPA. EPA has assumed
responsibility for maintaining a database of submitted RMPs, which
will be made available electronically to the implementing agency,
states, local governments, and (except for the Offsite Consequence
Analysis data) to the public. (2) Collecting and submitting
information to support petitions to modify the list of regulated
substances under CAA Section 112(r)(3). The regulations include
requirements for a petitioner to submit sufficient information in
support of a petition to scientifically support the request to add
or delete a chemical from the list of regulated substances. The
Agency will use this information in making the decision to grant or
deny a petition. This ICR amends the existing ICR in response to a
proposed rule to revise the existing rule codified in 40 CFR Part
68, and addresses the following information requirements that are
part of the proposed revision to the rule: (1) Hold a public
meeting within 90 days of an accident subject to reporting under
68.42. (2) Meet and coordinate with local responders to share
emergency response planning information. (3) Conduct an emergency
notification exercise to verify emergency contact information. (4)
Conduct and document emergency response field and tabletop
exercises.
The changes in cost and burden
in this ICR compared to the previous ICR are in response to
proposed revisions to an existing rule codified in 40 CFR Part 68.
The proposed rule changes include holding a public meeting within
90-days of an accident subject to reporting under 68.42, conducting
emergency drills and exercises, and coordinating response
activities with local responders.
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:
(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;
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.