Notice2025-18605

Agency Information Collection Activities; Submission to the Office of Management and Budget for Review and Approval; Comment Request; Risk Management Program Requirements and Petitions To Modify the List of Regulated Substances Under Section 112(r) of the Clean Air Act (Renewal)

Primary source

Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.

Published
September 25, 2025

Issuing agencies

Environmental Protection Agency

Abstract

The Environmental Protection Agency (EPA) has submitted an information collection request (ICR), Risk Management Program Requirements and Petitions to Modify the List of Regulated Substances the Clean Air Act (EPA ICR Number 1656.19, OMB Control Number 2050- 0144) to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act (PRA). This is a proposed extension of the ICR, which is currently approved through September 30, 2025. Public comments were previously requested via the Federal Register on April 17, 2025 during a 60-day comment period. This notice allows for an additional 30 days for public comments.

Full Text

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<title>Federal Register, Volume 90 Issue 184 (Thursday, September 25, 2025)</title>
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[Federal Register Volume 90, Number 184 (Thursday, September 25, 2025)]
[Notices]
[Pages 46196-46197]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2025-18605]


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ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OLEM-2015-0725; FRL-12996-01-OMS]


Agency Information Collection Activities; Submission to the 
Office of Management and Budget for Review and Approval; Comment 
Request; Risk Management Program Requirements and Petitions To Modify 
the List of Regulated Substances Under Section 112(r) of the Clean Air 
Act (Renewal)

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

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SUMMARY: The Environmental Protection Agency (EPA) has submitted an 
information collection request (ICR), Risk Management Program 
Requirements and Petitions to Modify the List of Regulated Substances 
the Clean Air Act (EPA ICR Number 1656.19, OMB Control Number 2050-
0144) to the Office of Management and Budget (OMB) for review and 
approval in accordance with the Paperwork Reduction Act (PRA). This is 
a proposed extension of the ICR, which is currently approved through 
September 30, 2025. Public comments were previously requested via the 
Federal Register on April 17, 2025 during a 60-day comment period. This 
notice allows for an additional 30 days for public comments.

DATES: Comments must be submitted on or before October 27, 2025.

ADDRESSES: Submit your comments, referencing Docket ID Number EPA-HQ-
OEM-2015-0725, to EPA online using <a href="http://www.regulations.gov">www.regulations.gov</a> (our preferred 
method) or by mail to: EPA Docket Center, Environmental Protection 
Agency, Mail Code 28221T, 1200 Pennsylvania Ave. NW, Washington, DC 
20460.
    EPA's policy is that all comments received will be included in the 
public docket without change including any personal information 
provided, unless the comment includes profanity, threats, information 
claimed to be Confidential Business Information (CBI) or other 
information whose disclosure is restricted by statute.
    Submit written comments and recommendations to OMB for the proposed 
information collection within 30 days of publication of this notice to 
<a href="http://www.reginfo.gov/public/do/PRAMain">www.reginfo.gov/public/do/PRAMain</a>. Find this particular information 
collection by selecting ``Currently under 30-day Review--Open for 
Public Comments'' or by using the search function.

FOR FURTHER INFORMATION CONTACT: William Noggle, Office of Emergency 
Management, Mail Code 5104A, Environmental Protection Agency, 1200 
Pennsylvania Ave. NW, Washington, DC 20460; telephone number: (202) 
566-1306; email address: <a href="/cdn-cgi/l/email-protection#4927262e2e252c673e202525202824092c3928672e263f"><span class="__cf_email__" data-cfemail="0e60616969626b2079676262676f634e6b7e6f20696178">[email&#160;protected]</span></a>.

SUPPLEMENTARY INFORMATION: This is a proposed extension of the ICR, 
which is currently approved through September 30, 2025. An agency may 
not conduct or sponsor and a person is not required to respond to a 
collection of information unless it displays a currently valid OMB 
control number.
    Public comments were previously requested via the Federal Register 
on April 17, 2025 during a 60-day comment period (90 FR 16126). This 
notice allows for an additional 30 days for public comments. Supporting 
documents, which explain in detail the information that the EPA will be 
collecting, are available in the public docket for this ICR. The docket 
can be viewed online at <a href="http://www.regulations.gov">www.regulations.gov</a> or in person at the EPA 
Docket Center, WJC West, Room 3334, 1301 Constitution Ave. NW, 
Washington, DC. The telephone number for the Docket Center is 202-566-
1744. For additional information about EPA's public docket, visit 
<a href="http://www.epa.gov/dockets">http://www.epa.gov/dockets</a>.
    Abstract: Information collection for on-site documentation of Risk 
Management Plans (RMPs) is authorized by Clean Air Act (CAA) sections 
112(r)(7)(B)(i) and (ii), which state, ``The Administrator shall 
promulgate reasonable regulations and appropriate guidance to provide . 
. . for the prevention and detection of accidental releases of 
regulated substances . . .'' and, ``The regulations . . . shall require 
the owner or operator . . . to prepare and implement a risk management 
plan to detect and prevent or minimize accidental releases . . .'' 
Information collection for submitting an RMP is authorized under CAA 
section 112(r)(7)(B)(iii), which states in relevant part, ``The, owner 
or operator of each stationary source . . . shall register a risk 
management plan . . . with the Administrator before the effective date 
of the regulations . . . in such form and manner as the Administrator 
shall, by rule, require . . . and shall be available to the public 
under section 114(c).'' Information collection for on-site

[[Page 46197]]

documentation and submittal of RMPs also is authorized by CAA section 
114(a)(1). State and local authorities use the information in RMPs to 
modify and enhance their community response plans. The agencies 
implementing the Risk Management Program use RMPs to evaluate 
compliance with the Chemical Accident Provisions in 40 CFR part 68 and 
to identify sources for inspection that may pose significant risks to 
the community. Citizens may use the information to assess chemical 
hazards in their communities.
    Form Numbers: None.
    Respondents/affected entities: Stationary sources that manufacture, 
react, mix, store, or use substances in processes that require 
equipment designed, constructed, installed, operated, or maintained in 
specific ways to prevent accidental releases and ensure safe 
operations.
    Respondent's obligation to respond: Mandatory under CAA section 
112(r)(7)(B)(iii).
    Estimated number of respondents: 14,513 (total).
    Frequency of response: Sources are required to register and submit 
an RMP once every five years unless there are significant changes in 
the information provided.
    Total estimated burden: 667,639 hours (per year). Burden is defined 
at 5 CFR 1320.03(b).
    Total estimated cost: $52,611,420 (per year), which includes 
$36,792 annual operation & maintenance costs.
    Changes in the estimates: There is decrease of 36,336 hours in the 
total estimated respondent burden compared with the ICR currently 
approved by OMB. Two primary reasons account for this decrease in 
burden. First, the burden varies from one ICR renewal to the next due 
to different resubmission deadlines based on the sources' RMP re-
submission deadlines and other regulatory deadlines. Therefore, the 
burden changes each year depending on how many sources must submit 
their RMP and comply with certain prevention program requirements. 
Second, the number of sources subject to the regulations fluctuates 
regularly and is slightly lower than in the previous ICR (12,074 vs. 
12,341 sources) due to the net change in new sources minus deregistered 
sources, as well as a lower number of new facilities anticipated to 
become subject to the RMP requirements during the three-year clearance 
period.

Courtney Kerwin,
Director, Information Engagement Division.
[FR Doc. 2025-18605 Filed 9-24-25; 8:45 am]
BILLING CODE 6560-50-P


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Indexed from Federal Register on September 25, 2025.

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