Change Requests

What is an ICR?

An Information Collection Request (ICR) is a federal agency's request for approval from the Office of Management and Budget (OMB) to collect information from the public. Under the Paperwork Reduction Act (PRA), agencies must justify why the information is needed and how it will be used.

When are they submitted?

Federal agencies are required to submit an ICR whenever they create, renew, modify an information collection. Each ICR includes a description of the collection, supporting materials and documentation (such as forms, surveys, or scripts), and proof that the agency has met the requirements of the PRA.

The ICR is submitted to the The Office of Information and Regulatory Affairs (OIRA) within OMB for review and approval. OIRA grants approval for a maximum of three years, after which the collection must be renewed through a new ICR submission.

Where to find an ICR?

ICRs are publicly available on RegInfo.gov, and additional guidance can be found in the FAQs.

Note: Presidential Action influences are notated for ICRs received between January 20, 2025 and July 19, 2025.

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Presidential Action Driven

Showing 25 of 15045 results

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Title
Reference Number
OMB Control Number
Agency
Received
Concluded
Action
Status
Request Type
Presidential Action

Title:

FERC-725R, RD25-5 Mandatory Reliability Standards: BAL Reliability Standards

Reference Number:

202507-1902-003

Omb Control Number:

1902-0268

Agency:

FERC

Received:

2025-07-30

Concluded:

2025-11-20

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
FERC-725R, RD25-5 Mandatory Reliability Standards: BAL Reliability Standards

Key Information

Abstract

The FERC 725R consists of BAL standards. These standards pertain to resource and demand balancing (BAL) body of standards and detail the role of entities to ensure proper load, generation, and interchange balancing. At present, FERC-725R consists of a collection of information associated with the following nationwide Reliability Standards: • BAL-001-2, Real Power Balancing Control Performance; • BAL-002-3, Disturbance Control Standard – Contingency Reserve for Recovery from a Balancing Contingency Event; and • BAL-003-2, Frequency Response and Frequency Bias Setting; and • BAL-005-1, Balancing Authority Control. • BAL-007-1, Near-term Energy Reliability Assessments (ERA)

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

16 USC 824o
View Law

Presidential Action:

-

Title:

Tropical Disease Priority Review Vouchers

Reference Number:

202501-0910-009

Omb Control Number:

0910-0822

Agency:

HHS/FDA

Received:

2025-07-30

Concluded:

2025-12-30

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Tropical Disease Priority Review Vouchers

Key Information

Abstract

This information collection supports implementation of section 524 of the Federal Food, Drug, and Cosmetic Act. The statute provides FDA with authority for awarding priority review vouchers for future applications to sponsors of tropical disease product applications that meet the criteria specified by the Act. We have also developed associated guidance intended to explain to internal and external stakeholders how we implement the provisions of section 524.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

21 USC 524
View Law
Pub.L. 115 - 52 611
View Law

Presidential Action:

-

Title:

Construction-Manager-as-Constructor Contracting; GSAR Section Affected: 552.236-72

Reference Number:

202504-3090-008

Omb Control Number:

3090-0308

Agency:

GSA

Received:

2025-07-30

Concluded:

2025-09-08

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Construction-Manager-as-Constructor Contracting; GSAR Section Affected: 552.236-72

Key Information

Abstract

The collected information is required by GSAR clause 552.236-72, Submittals. The GSAR clause requires the Contractor to prepare and submit all submittals as specified in the contract or requested by the Contracting Officer in solicitations and contracts if construction, dismantling, demolition, or removal of improvements is contemplated. Alternate I of the clause will be used when a design-build project delivery method will be followed. ● Submittals. Submittals may include safety plans, schedules, shop drawings, coordination drawings, samples, calculations, product information, or mockups. ● Shop Drawings. Shop drawings may include fabrication, erection and setting drawings, manufacturers' scale drawings, wiring and control diagrams, cuts or entire catalogs, pamphlets, descriptive literature, and performance and test data. ● Additional information. Unless otherwise provided in this contract, or otherwise directed by the Contracting Officer, submittals shall be submitted to the Contracting Officer: (i) The Contractor shall be entitled to receive notice of action on submittals within a reasonable time, given the volume or complexity of the submittals and the criticality of the affected activities to substantial completion as may be indicated in the project schedule (ii) The Contractor shall not proceed with construction work or procure products or materials described or shown in submittals until the submittal is reviewed. Any work or activity undertaken prior to review shall be at the Contractor's risk. Should the Contracting Officer subsequently determine that the work or activity does not comply with the contract, the Contractor shall be responsible for all cost and time required to comply with the Contracting Officer's determination. The Contracting Officer shall have the right to order the Contractor to cease execution of work for which submittals have not been reviewed. The Government shall not be liable for any cost or delay incurred by the Contractor attributable to the proper exercise of this right. See Item 6 below for the consequences if the information collection is not conducted or conducted less frequently.

Federal Register Notices

60-Day FRN
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30-Day FRN
View Notice

Presidential Action:

-

Title:

Food Labeling: Notification Procedures for Statements on Dietary Supplements

Reference Number:

202411-0910-001

Omb Control Number:

0910-0331

Agency:

HHS/FDA

Received:

2025-07-30

Concluded:

2025-09-02

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Food Labeling: Notification Procedures for Statements on Dietary Supplements

Key Information

Abstract

The reporting requirements of this regulation implement the Dietary Supplement Health and Education Act. The subject regulation establishes reporting procedures necessary to inform FDA when dietary supplement manufacturers are making statements of nutritional support on their labels or in their labeling. FDA is seeking OMB approval of an electronic submission method for this collection.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

21 USC 343(r)(6)
View Law

Presidential Action:

-

Title:

Application for grants under the Strengthening Institutions Program, CFDA# 84.031A & 84.031F

Reference Number:

202507-1840-001

Omb Control Number:

1840-0114

Agency:

ED/OPE

Received:

2025-07-30

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
Application for grants under the Strengthening Institutions Program, CFDA# 84.031A & 84.031F

Key Information

Abstract

This request is for an extension of the application booklet for the Strengthening Institutions Program (SIP), Assistance Listing Numbers (ALN) # 84.031A and 84.031F. SIP provides grants to eligible institutions of higher education (IHEs) to improve their academic programs, institutional management, and fiscal stability to increase their self-sufficiency and strengthen their capacity. Funding is targeted to institutions that enroll a large proportion of financially disadvantaged students and have low per-student expenditures. Section 311(b) and Section 391(a)(1) of Title III, Part A of the Higher Education Act of 1965, as amended (HEA), 20 US Code Section 1057 and the governing regulations (34 CFR 607.1-607.31) require collection of the information identified in the application package prior to any new awards being made.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

20 USC 1057
View Law

Presidential Action:

-

Title:

Export Notification and Recordkeeping Requirements

Reference Number:

202507-0910-003

Omb Control Number:

0910-0482

Agency:

HHS/FDA

Received:

2025-07-30

Concluded:

2025-09-02

Action:

Approved without change

Status:

Active

Request Type:

Reinstatement with change of a previously approved collection
Export Notification and Recordkeeping Requirements

Key Information

Abstract

The information collection supports FDA regulations at 21 CFR 1.101 and pertains to the notifications and records required for human drug, biological product, device, animal drug, food, cosmetic, and tobacco product exports under sections 801 or 802 of the Federal Food, Drug, and Cosmetic Act or (21 U.S.C. 381 and 382) or section 351 of the Public Health Service Act (42 U.S.C. 262).

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

42 USC 262
View Law
21 USC 301, et. seq.
View Law

Presidential Action:

-

Title:

FERC-725A, RD25-5 Mandatory Reliability Standards for the Bulk-Power System

Reference Number:

202507-1902-004

Omb Control Number:

1902-0244

Agency:

FERC

Received:

2025-07-30

Concluded:

2025-11-20

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
FERC-725A, RD25-5 Mandatory Reliability Standards for the Bulk-Power System

Key Information

Abstract

The FERC 725A contains the Transmission Operations (TOP) standards and Interchange Scheduling and Coordination (INT) Standards that pertain to operation planning for transmission providers. TOP-001, TOP-002, TOP-003, TOP-010, INT-006, and INT-009. In this ICR, the Commission is approving TOP-003-7.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

16 USC 824o
View Law

Presidential Action:

-

Title:

Compounding Animal Drugs from Bulk Drug Substances

Reference Number:

202507-0910-011

Omb Control Number:

0910-0904

Agency:

HHS/FDA

Received:

2025-07-30

Concluded:

2025-09-02

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Compounding Animal Drugs from Bulk Drug Substances

Key Information

Abstract

This information collection accounts for burden that may be attendant to recommendations discussed in FDA guidance applicable to pharmacists and veterinarians who compound animal drugs from bulk drug substances.

Federal Register Notices

60-Day FRN
View Notice
30-Day FRN
View Notice

Presidential Action:

-

Title:

Drivers’ Use of Camera-Based Rear Visibility Systems Versus Traditional Mirrors

Reference Number:

202506-2127-003

Omb Control Number:

2127-0756

Agency:

DOT/NHTSA

Received:

2025-07-30

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
Drivers’ Use of Camera-Based Rear Visibility Systems Versus Traditional Mirrors

Key Information

Abstract

The National Highway Traffic Safety Administration (NHTSA) has proposed to perform research involving the collection of information from the public as part of a multi-year effort to learn about drivers’ use of camera-based rear visibility systems as compared to their use of traditional vehicle outside mirrors. This research will support NHTSA in evaluating whether to pursue a regulation modification that would permit technologies other than mirrors, such as camera-based visibility systems (sometimes referred to as camera monitor systems (CMS)), for compliance with FMVSS No. 111. The data collections will be performed once to obtain the target number of valid test participants. Study participants will be members of the general public and participation will be voluntary. Participants will include licensed car and/or commercial truck drivers aged 25 to 65, who are healthy and able to drive without assistive devices. Participants will be recruited using print and online newspaper advertisements. Study participation will be voluntary and monetary compensation will be provided. The research will be conducted in two parts. Data collection will begin upon receipt of PRA clearance and will first involve light vehicles, and a second, subsequent part will involve heavy trucks. Participants will drive a production vehicle equipped with a commercially available or prototype camera-based visibility system in place of outside mirrors and a vehicle equipped with an original equipment mirror system. The research will involve track-based and on-road, semi-naturalistic driving experimentation. Vehicles used in testing will be equipped with instrumentation for recording driver eye-glance behavior, as well as vehicle speed, position, steering angle, and turn signal status. Sensors will also be used to determine and record the distances between the test vehicle and surrounding vehicles during testing. Information will be collected over the course of the research through participant recruitment screening questions, observation of driving behaviors, and post-drive questionnaires. Questions addressed to individuals will serve to assess individuals’ suitability for study participation, to obtain feedback regarding participants’ use of the CMS, and to gauge individuals’ level of comfort with and confidence in the CMS performance and safety.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

49 USC 301
View Law

Presidential Action:

-

Title:

Nuclear Material Events Database (NMED) for the Collection of Event Report, Response, Analyses, and Follow-up Data on Events Involving the Use of Atomic Energy Act Radioactive Byproduct Material

Reference Number:

202507-3150-005

Omb Control Number:

3150-0178

Agency:

NRC

Received:

2025-07-30

Concluded:

2025-12-29

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Nuclear Material Events Database (NMED) for the Collection of Event Report, Response, Analyses, and Follow-up Data on Events Involving the Use of Atomic Energy Act Radioactive Byproduct Material

Key Information

Abstract

NRC regulations require NRC licensees to report incidents and over exposures, leaking or contaminated sealed source(s), release of excessive contamination of radioactive material, lost or stolen radioactive material, equipment failures, abandoned well logging sources and medical events. Agreement State licenses are also required to report these events to their individual Agreement State regulatory authorities under compatible Agreement State regulations. The NRC is requesting that the Agreement States provide information to NRC on the initial notification, response actions, and follow-up investigations on events involving the use (including suspected theft or terrorist activities) of nuclear materials regulated pursuant to the Atomic Energy Act. The event information should be provided in a uniform electronic format, for assessment and identification of any facilities/site specific or generic safety concerns that could have the potential to impact public health and safety. The identification and review of safety concerns may result in lessons learned, and may also identify generic issues for further study which could result in proposals for changes or revisions to technical or regulatory designs, processes, standards, guidance or requirements.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

Pub.L. 83 - 703 1-311
View Law

Presidential Action:

-

Title:

Stem Cell Therapeutic Outcomes Database

Reference Number:

202507-0915-003

Omb Control Number:

0915-0310

Agency:

HHS/HSA

Received:

2025-07-30

Concluded:

2025-09-03

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Stem Cell Therapeutic Outcomes Database

Key Information

Abstract

The Stem Cell Therapeutic and Research Act of 2005 (Public Law 109-129, December 20, 2005) as amended and codified in Section 379A of the Public Health Service Act (42 U.S.C. 247l), provides for the collection and maintenance of human blood stem cells for the treatment of patients and research. The Public Health Service Act requires the Secretary of HHS to contract for the establishment and maintenance of information related to patients who have received stem cell therapeutic products and to do so using an electronic format. HRSA has established the Stem Cell Therapeutic Outcomes Database (SCTOD), a component of the C.W. Bill Young Cell Transplantation Program (Program), which necessitates certain electronic record-keeping and reporting requirements to perform functions related to hematopoietic stem cell transplantation (HCT) under contract to HHS. Data are collected from transplant centers by the Center for International Blood and Marrow Transplant Research. They are used for ongoing analysis of transplant outcomes to improve treatment and survival for patients who may benefit from cellular therapies.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

Pub.L. 117 - 15 2
View Law
Pub.L. 111 - 264 2
View Law
Pub.L. 114 - 104 2
View Law
42 USC 247k, section 379
View Law

Presidential Action:

-

Title:

Medical Device Reporting

Reference Number:

202412-0910-004

Omb Control Number:

0910-0437

Agency:

HHS/FDA

Received:

2025-07-30

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Reinstatement with change of a previously approved collection
Medical Device Reporting

Key Information

Abstract

This ICR collects information from medical device manufacturers, importers, and user facilities that are required to submit electronic and paper medical device reports (MDRs) to the Food and Drug Administration (FDA) and to maintain records, and who may also seek exemption from these requirements. The information that is obtained from these reports will be used to evaluate risks associated with medical devices and enable FDA to take appropriate regulatory measures to protect the public health. Complete, accurate, and timely adverse event information is necessary for the identification of emerging device problems so the Agency can protect the public health under the FD&C Act.

Federal Register Notices

60-Day FRN
View Notice
30-Day FRN
View Notice

Authorizing Statutes

21 USC 519(a)(1)(B)(ii)
View Law
21 USC 360i(a)(b)(c)
View Law

Presidential Action:

-

Title:

Tobacco Products, User Fees, Requirements for the Submission of Data Needed to Calculate User Fees for Domestic Manufacturers and Importers of Tobacco Products

Reference Number:

202507-0910-002

Omb Control Number:

0910-0749

Agency:

HHS/FDA

Received:

2025-07-30

Concluded:

2025-09-02

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Tobacco Products, User Fees, Requirements for the Submission of Data Needed to Calculate User Fees for Domestic Manufacturers and Importers of Tobacco Products

Key Information

Abstract

The Food and Drug Administration (FDA) is issuing a final rule that requires domestic manufacturers and importers of cigars and pipe tobacco to submit information needed to calculate the amount of user fees assessed under the Federal Food, Drug, and Cosmetic Act (the FD&C Act). FDA recently expanded its authority by issuing a final rule, “Deeming Tobacco Products To Be Subject to the Federal Food, Drug, and Cosmetic Act, as Amended by the Family Smoking Prevention and Tobacco Control Act; Restrictions on the Sale and Distribution of Tobacco Products and Required Warning Statements for Tobacco Products” (Deeming rule), deeming all products that meet the statutory definition of “tobacco product,” except accessories of the newly deemed tobacco products, to be subject to the FD&C Act. The Deeming rule, among other things, subjected domestic manufacturers and importers of cigars and pipe tobacco to the FD&C Act’s user fee requirements. Consistent with the Deeming rule and the requirements of the FD&C Act, this final rule requires the submission of the information needed to calculate user fee assessments for each manufacturer and importer of cigars and pipe tobacco to FDA.

Federal Register Notices

60-Day FRN
View Notice
30-Day FRN
View Notice

Authorizing Statutes

Pub.L. 111 - 31 31
View Law

Presidential Action:

-

Title:

PHS Guideline on Infectious Disease Issues in Xenotransplantation

Reference Number:

202507-0910-010

Omb Control Number:

0910-0456

Agency:

HHS/FDA

Received:

2025-07-30

Concluded:

2025-09-16

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
PHS Guideline on Infectious Disease Issues in Xenotransplantation

Key Information

Abstract

This information collection supports implementation of sections 351 and 361 of the Public Health Service Act (PHS Act) (42 U.S.C. 262 and 264) and certain drug provisions of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301 et seq.), regarding xenotransplantation. As set forth in the “PHS Guideline on Infectious Disease Issues in Xenotransplantation,” guidelines were developed by the Public Health Service (PHS) to identify general principles for the prevention and control of infectious diseases associated with xenotransplantation that may pose a risk to public health. The PHS guideline recommends procedures to diminish the risk of transmission of infectious agents to the xenotransplantation product recipient and to the general public.

Federal Register Notices

60-Day FRN
View Notice
30-Day FRN
View Notice

Authorizing Statutes

21 USC 301
View Law
42 USC 264
View Law
42 USC 262
View Law

Presidential Action:

-

Title:

30 CFR Part 773 - Requirements for Permits and Permit Processing

Reference Number:

202501-1029-003

Omb Control Number:

1029-0115

Agency:

DOI/OSMRE

Received:

2025-07-30

Concluded:

2025-12-30

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
30 CFR Part 773 - Requirements for Permits and Permit Processing

Key Information

Abstract

The collection activities for this Part ensure that the public has the opportunity to review permit applications prior to their approval, and that applicants for permanent program permits or their associates who are in violation of the Surface Mining Control and Reclamation Act do not receive surface coal mining permits pending resolution of their violations. This collection request includes permit applicant processing fees in Federal Program States and on Indian lands.

Federal Register Notices

60-Day FRN
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30-Day FRN
View Notice

Authorizing Statutes

30 USC 1201 et seq.
View Law

Presidential Action:

-

Title:

Benefit Rights and Experience Report

Reference Number:

202507-1205-001

Omb Control Number:

1205-0177

Agency:

DOL/ETA

Received:

2025-07-30

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
Benefit Rights and Experience Report

Key Information

Abstract

The data in the ETA 218, Benefit Rights and Experience Report, includes numbers of individuals who were and were not monetarily eligible, those eligible for the maximum benefits, those eligible based on classification by potential duration categories, and those exhausting their full entitlement as classified by actual duration categories. This data is collected as part of the initial claim process. It is transmitted electronically to the National Office on a quarterly basis. This data is used by the National Office in solvency studies, cost estimating and modeling, and to assess State benefit formulas. If this data were not available, cost estimating and modeling would be less accurate.

Federal Register Notices

60-Day FRN
View Notice
30-Day FRN
View Notice

Authorizing Statutes

42 USC 503(a)(6)
View Law

Presidential Action:

-

Title:

2026-2027 Free Application for Federal Student Aid (FAFSA)

Reference Number:

202507-1845-005

Omb Control Number:

1845-0001

Agency:

ED/FSA

Received:

2025-07-30

Concluded:

2025-07-30

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
2026-2027 Free Application for Federal Student Aid (FAFSA)

Key Information

Abstract

Section 483 of the Higher Education Act of 1965, as amended (HEA), mandates that the Secretary of Education “…shall produce, distribute, and process free of charge common financial reporting forms as described in this subsection to be used for application and reapplication to determine the need and eligibility of a student for financial assistance...”. The determination of need and eligibility are for the following Title IV, HEA, federal student financial assistance programs: the Federal Pell Grant Program; the Campus-Based programs (Federal Supplemental Educational Opportunity Grant (FSEOG) and Federal Work-Study (FWS)); the William D. Ford Federal Direct Loan (Direct Loan) Program; the Teacher Education Assistance for College and Higher Education (TEACH) Grant; and the Children of Fallen Heroes Scholarship. Federal Student Aid (FSA), an office of the U.S. Department of Education (the Department), subsequently developed an application process to collect and process the data necessary to determine a student’s eligibility to receive Title IV, HEA program assistance. The application process involves an applicant’s submission of the Free Application for Federal Student Aid (FAFSA®). After submission and processing of the FAFSA form, an applicant receives a FAFSA Submission Summary, which is a summary of the processed data they submitted on the FAFSA form. The applicant reviews the summary, and, if necessary, will make corrections or updates to their submitted FAFSA data. Institutions of higher education listed by the applicant on the FAFSA form also receive a summary of processed data submitted on the FAFSA form, which is called the Institutional Student Information Record (ISIR). The specific questions that applicants are asked to answer in the application process are described separately in the Data Elements and Justification document. The document identifies the data elements associated with each FAFSA question and provides the justification for including each question on the FAFSA form. In addition to the calculation of financial need for the various Title IV programs, the FAFSA form also collects data that allows for a determination of an applicant’s eligibility for state and institutional financial aid programs. If these data elements were not collected, the Department and institutions of higher education would be unable to make a determination of financial need and subsequently would be unable to award any Title IV, HEA program assistance, as mandated by the HEA. Many states would also be greatly hindered in their calculation of state aid to applicants. This is a request for revisions of a current information collection, and important changes to the FAFSA form are described separately in the 2026-27 Summary of Enhancements document.Emergency Justfication:The OBBBA was signed into law on July 4, 2025. The Act made changes to the FAFSA for the 2026-27 award year. The Department would not have been able to make these changes prior to the enactment of the OBBBA. Because of this, obtaining full OMB clearance to use the most accurate version of the FAFSA prior to FAFSA beta testing and FAFSA launch would not be possible. The FAFSA form is scheduled to be launched by October 1,2025 for the 2026-2027 award year. Without emergency review of an updated FAFSA form, beta testing and the launch of the FAFSA would be delayed. This means that students would not be able to complete a FAFSA form to determine eligibility for federal student aid. Institutions of higher education would not be able to package aid for their students until their students’ FAFSA forms have been processed. These delays would cause the FAFSA form to not be available to the public on time. Applicants and schools rely on the on-time launch of the FAFSA form each year. Delays could impact institutional enrollment projections, student enrollment, and student decisions to apply for federal student aid.

Federal Register Notices

60-Day FRN
View Notice
30-Day FRN
View Notice

Authorizing Statutes

20 USC 1090
View Law

Presidential Action:

-

Title:

Motor Carrier Identification Report

Reference Number:

202507-2126-003

Omb Control Number:

2126-0013

Agency:

DOT/FMCSA

Received:

2025-07-29

Concluded:

2025-09-05

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Motor Carrier Identification Report

Key Information

Abstract

The information collection is mandatory reporting requirements and consists of 3 information collection instruments. IC-1, Form MCS-150, Motor Carrier Identification Report is filed by all motor carriers conducting operations in interstate or international commerce before beginning operations. It is also used by motor carriers needing to update previously submitted information, and on a biennial update basis. IC-2, Form MCS-150B, Combined Motor Carrier Identification and HM Permit Application is filed by interstate motor carriers that transport the permitted hazardous materials. It is also used by motor carriers needing to update previously submitted information, and on a biennial update basis. IC-3, Form MCS-150C, Intermodal Equipment Provider Identification Report is filed by IEPs that interchange intermodal equipment with a motor carrier or have contractual responsibility for the maintenance of the intermodal equipment. FMCSA uses the information to identify its regulated entities, to help prioritize the Agency’s enforcement activities, to aid in assessing the safety outcomes of those activities, and for statistical purposes. This information collection supports the agency’s strategic goal of safety by establishing and monitoring safe operating requirements for motor carriers, commercial motor vehicle drivers, vehicles, and vehicle equipment.

Federal Register Notices

60-Day FRN
View Notice
30-Day FRN
View Notice

Authorizing Statutes

Pub.L. 107 - 87 115 Stat.. 833
View Law
Pub.L. 104 - 88 100 Stat. 803
View Law

Presidential Action:

-

Title:

Disqualification Proceedings

Reference Number:

202503-2130-004

Omb Control Number:

2130-0529

Agency:

DOT/FRA

Received:

2025-07-29

Concluded:

2025-12-05

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Disqualification Proceedings

Key Information

Abstract

FRA regulations at 49 CFR part 209, subpart D, explain FRA’s responsibilities, and the rights and responsibilities of railroads and railroad employees, regarding disqualification procedures. FRA uses the information collected to promote and maintain rail safety by ensuring that disqualified individuals do not serve in safety-sensitive positions. This collection of information is mandatory, collected as needed, and it involves reporting requirements.

Federal Register Notices

60-Day FRN
View Notice
30-Day FRN
View Notice

Authorizing Statutes

49 USC 20103
View Law
Pub.L. 100 - 342 3
View Law

Presidential Action:

-

Title:

Hours of Service (HOS) of Drivers Regulations

Reference Number:

202507-2126-005

Omb Control Number:

2126-0001

Agency:

DOT/FMCSA

Received:

2025-07-29

Concluded:

2025-08-21

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Hours of Service (HOS) of Drivers Regulations

Key Information

Abstract

This non-substantive change request on OMB Control No. 2126-0001 corrects the CFR citations in the two information collections. The Hours of Service (HOS) rules apply to both property and passenger motor carriers. The HOS rules set limits on the on-duty time and driving time of CMV drivers, and mandate the amount and frequency of the time off-duty that such drivers must receive. Two types of information are collected under this IC: (1) drivers’ daily record of duty status (RODS) (electronic records or, in some cases, paper logbooks), and (2) supporting documents, such as fuel and toll receipts, that may be used by motor carriers to verify the accuracy of the RODS and to document expense deductions taken in the determination of taxable income. The information is collected on an annual basis. The purpose of the collection of the RODS and supporting documents of the HOS rules is to provide the Agency with its most effective tool in combating driver fatigue. Enforcement officials at roadside employ the RODS and supporting documents to determine the amount of time a driver has spent off duty prior to the driver’s current duty day. They also determine the amount of time the driver has been on duty that duty day, and the amount of time the driver has been behind the wheel driving during the duty day. Enforcement officials examine the RODS for seven of the immediately preceding days to determine compliance with the HOS rules. The RODS are an invaluable tool used to detect inaccurate and falsified logs that facilitates removing fatigued, unsafe drivers off the road. Enforcement officials employ the RODS and supporting documents retained by the motor carrier when conducting on-site investigative reviews of motor carriers. The safety assessments that result from such reviews are public information, and many shippers routinely examine the assessments, as well as crash and regulatory compliance records, when selecting a motor carrier. The Motor Carrier Safety Assistance Program (MCSAP) requires States, as a condition of receiving grant funding, to adopt and enforce State CMV safety laws and regulations that are compatible with the FMCSRs and these include the HOS rules. States embrace the Federal enforcement scheme for regulating safety in the operation of CMVs, and work closely with Federal investigators in enforcing the HOS rules. Motor carriers also help FMCSA detect fatigued drivers. It is in their interest to be proactive in detecting inaccuracy or falsification of RODS by their CMV drivers to avoid the penalties resulting from such infractions. Replacing paper RODS with electronic RODS enhances the accuracy and minimizes the falsification of RODS. Motor carriers will continue to examine the supporting documents, such as fuel receipts, toll receipts, bills of lading, repair invoices, and compare them to the entries on the RODS. Comparing supporting documents to the RODS helps the motor carrier verify the accuracy of the HOS reported by their CMV drivers. Motor carrier use of the RODS and driver-supplied supporting documents enhances driver adherence to the HOS rules, keeps fatigued drivers off the road, and helps FMCSA protect the public. This ICR supports the Department of Transportation’s Strategic Goal of Safety because the information helps the Agency improve the safety of drivers operating CMVs on our Nation’s highways.

Federal Register Notices

60-Day FRN
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Authorizing Statutes

49 USC 31502
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49 USC 31136
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49 USC 522
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49 USC 521
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49 USC 526
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Presidential Action:

-

Title:

Business Trends and Outlook Survey

Reference Number:

202507-0607-004

Omb Control Number:

0607-1022

Agency:

DOC/CENSUS

Received:

2025-07-29

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

No material or nonsubstantive change to a currently approved collection
Business Trends and Outlook Survey

Key Information

Abstract

The Business Trends and Outlook Survey (BTOS) will be a new experimental survey with bi-weekly data collection and publication. This continuous near real time data publication will provide a baseline of the U.S. economy and will measure change as a result of current and future economic shocks. The ongoing nature of the BTOS is in response to stakeholder feedback on the Small Business Pulse Survey (SBPS), which was that economic baseline or ‘norms’ data would have been helpful to have in comparison to the SBPS data on pandemic impact.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

13 USC 131, 182
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Presidential Action:

-

Title:

Part C and Part D Medicare Prescription Payment Plan Model Documents (CMS-10882) - IRA

Reference Number:

202507-0938-023

Omb Control Number:

0938-1475

Agency:

HHS/CMS

Received:

2025-07-29

Concluded:

2025-12-22

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Part C and Part D Medicare Prescription Payment Plan Model Documents (CMS-10882) - IRA

Key Information

Abstract

The purpose of this information collection request for the approval of model documents for the Medicare Prescription Drug Program (Part D) is to meet the requirements of Section 11202 of the Inflation Reduction Act of 2022, Public L. 117-169 (IRA), which established the Medicare Prescription Payment Plan Program. Under this program, MA Organizations offering Part D coverage and Part D sponsors are required to offer enrollees the option to pay their Part D cost sharing in monthly amounts spread out over the plan year based on the formula described in section 1860D-2(b)(2)(E)(iv) of the Act. There are several education and outreach requirements for plan sponsors related to implementation of this program. The proposed documents in this information collection are designed to assist Part D plan sponsors and MA organizations in complying with Sections 1860D-2(b)(2)(E)(v)(II) – (IV) of the Social Security Act (the Act), which set forth the education and outreach responsibilities for Part D sponsors and MA organizations for this program. CMS has developed the six materials in the attached package as model notices to provide standardized and consistent language for potential and active program participants, regardless of which Part D plan they may be enrolled in. CMS will require Part D plans to disseminate these notices, as appropriate, to Part D enrollees to fulfill the requirements of the Sections 1860D-2(b)(2)(E)(v)(II) – (IV) of the Act. The six model notices and their related burden are accounted for in this PRA package. By providing these model notices, CMS is providing standardized messaging for all Part D beneficiaries and reducing administrative burden on Part D sponsors and MA organizations.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

Pub.L. 117 - 169 11202
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Presidential Action:

-

Title:

Foreign Supplier Verification Programs for Importers of Food for Humans and Animals

Reference Number:

202507-0910-001

Omb Control Number:

0910-0752

Agency:

HHS/FDA

Received:

2025-07-29

Concluded:

2025-09-15

Action:

Approved without change

Status:

Active

Request Type:

Reinstatement without change of a previously approved collection
Foreign Supplier Verification Programs for Importers of Food for Humans and Animals

Key Information

Abstract

The FSVP regulations require importers of most imported foods to take steps to verify that the foods they import into the United States are produced so they are safe and properly labeled with respect to allergens. These regulations are intended to work in tandem with other provisions of FSMA and the FD&C Act to create a more seamless system of food safety to protect U.S. consumers. Respondents to the collection are persons who import food into the United States subject to agency regulations.

Federal Register Notices

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30-Day FRN
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Authorizing Statutes

Pub.L. 111 - 353 301
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Presidential Action:

-

Title:

Project Abstract Summary

Reference Number:

202507-3041-003CF

Omb Control Number:

4040-0019

Agency:

CPSC

Received:

2025-07-29

Concluded:

2025-07-31

Action:

Approved without change

Status:

Active

Request Type:

RCF New
Project Abstract Summary

Key Information

Presidential Action:

-

Title:

Contractor Information Worksheet; GSA Form 850

Reference Number:

202507-3090-002

Omb Control Number:

3090-0283

Agency:

GSA

Received:

2025-07-29

Concluded:

2025-09-08

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Contractor Information Worksheet; GSA Form 850

Key Information

Abstract

Information collected through the Contractor Information Worksheet is necessary to meet: ● The Office of Management and Budget (OMB) Guidance M-05-24 for Homeland Security Presidential Directive (HSPD) 12 which authorizes Federal departments and agencies to ensure that contractors/their employees have limited/controlled access to facilities and information systems, and ● GSA Directive CIO P 2181.1 Homeland Security Presidential Directive-12 Personal Identity Verification and Credentialing which states that GSA contractors/their employees must undergo a minimum of a FBI National Criminal Information Check (NCIC) to receive unescorted physical access. GSA requires the collection of the information in the Contractor Information Worksheet to authorize and initiate background check requests for GSA contractor employees and for them to obtain a GSA access card. The background checks are carried out by the Office of Personnel Management, Facilities, Security & Contracting-Personnel Security (OPM FSC) and the credentialing process is carried out by the GSA’s Managed Service Office (MSO) in accordance with the terms and conditions of separate Memoranda of Agreement (MOAs). 2. Use of the Information. The GSA requesting official, referred to as “Sponsor,” collects and inputs the Contractor Information Worksheet data into the GSA Credential and Identity Management System (GCIMS). GSA Office of Mission Assurance (OMA) Identity, Credential and Access Management (ICAM) Division then uploads the relevant contractor data from GCIMS to the OPM e-QIP system for initiation of the contractor background investigation process. GCIMS automatically sends relevant data to the MSO for enrollment, including digital fingerprints for investigation and GSA access card, if needed. The OPM FSC performs the required background checks for GSA contractor employees once the applicant completes the e-QIP and fingerprinting process. The requesting official is responsible for requesting the investigation and/or GSA access card. Often the GSA requesting official is the Contracting Officer’s Representative (COR) for the contract, but this role may be fulfilled by a project manager, Public Buildings Service (PBS) building manager, or local Access Card Point of Contact (POC) as appropriate. If the applicant has a prior background check, OPM FSC uses the information in e-QIP to verify the prior determination. When OPM FSC makes an access determination, they notify the OMA ICAM Division. The OMA ICAM Division will input the results into GCIMS and notify the applicant, GSA sponsor, GSA POCs, and contractor’s point of contact.

Federal Register Notices

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30-Day FRN
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Presidential Action:

-
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