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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Showing 25 of 15032 results

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

Title:

CAHPS Home Health Care Survey (CMS-10275)

Reference Number:

202512-0938-004

Omb Control Number:

0938-1066

Agency:

HHS/CMS

Received:

2025-12-02

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
CAHPS Home Health Care Survey (CMS-10275)

Key Information

Abstract

As part of the DHHS Transparency Initiative on Quality Reporting, CMS plans to implement a process to measure and publicly report patients' experiences with home health care they receive from Medicare-certified home health agencies through the data collection effort described in this request: the Consumer Assessment of Healthcare Providers and Systems (CAHPS) Home Health Care Survey. The Home Health Care CAHPS Survey, which was developed and tested by the Agency for Healthcare Research and Quality (AHRQ) and is part of the family of CAHPS surveys, is a standardized survey for home health patients to assess their home health care providers and the quality of the home health care they receive. Prior to the Home Health Care CAHPS survey, there was no national standard for collecting data about home health care patients' experience with their home health care. This is a revision to the original PRA package which covered the voluntary implementation of the survey among Medicare-certified agencies and a randomized mode experiment to test the impact of different modes of data collection on survey responses. This is a revised PRA package because it now includes the burden to the home health agencies (HHAs) to contract with an approved HHCAHPS survey vendor to administer the HHCAHPS survey on their behalf.

Federal Register Notices

60-Day FRN
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Authorizing Statutes

42 USC 301
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Presidential Action:

-

Title:

Payment Default Report

Reference Number:

202512-3048-001

Omb Control Number:

3048-0028

Agency:

EXIMBANK

Received:

2025-12-02

Concluded:

2026-01-28

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Payment Default Report

Key Information

Abstract

The Export-Import Bank as part of its continuing effort to reduce paperwork and respondent burden, will use the Payment Default Report to allow insured/guaranteed parties and insurance brokers to report overdue payments from the borrower and/or guarantor. Ex-Im Bank customers have the option of submitting this form electronically through Ex-Im Online. Ex-Im Bank has simplified reporting of payment defaults in this form by including checkboxes and in the electronic version provided form some data fields to be self-populated.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

12 USC 635
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Presidential Action:

-

Title:

Credit Guarantee Facility Disbursement Approval Request

Reference Number:

202512-3048-002

Omb Control Number:

3048-0046

Agency:

EXIMBANK

Received:

2025-12-02

Concluded:

2026-01-28

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Credit Guarantee Facility Disbursement Approval Request

Key Information

Abstract

The Export Import Bank of the United States (Ex-Im Bank) pursuant to the Export Import Bank Act of 1945, as amended (12 USC 635, et seq), facilitates the finance of export of U.S. goods and services. By neutralizing the effect of export credit insurance and guarantees offered by foreign governments and by absorbing credit risks that the private sector will not accept, Ex-Im Bank enables U.S. exporters to complete fairly in foreign markets on the basis of price and product. This collection of information is necessary, pursuant to 12 USC Sec. 635 (a) (1), to determine eligibility of the export for Ex-Im Bank assistance. This form will enable Ex-Im Bank to identify the specific details of the export transaction. These details are necessary for determining the eligibility of disbursements for approval. Ex-Im Bank staff review this information to assist in determining that each disbursement under a Credit Guarantee Facility meets all of the terms and conditions for approval.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

12 USC 635
View Law

Presidential Action:

-

Title:

Investigational New Drug Regulations

Reference Number:

202509-0910-004

Omb Control Number:

0910-0014

Agency:

HHS/FDA

Received:

2025-12-02

Concluded:

2025-12-30

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Investigational New Drug Regulations

Key Information

Abstract

This information collection supports FDA implementation of regulations regarding investigational new drug applications. Respondents to the information collection are those who undertake clinical investigations of products that are subject to section 505 of the Federal Food, Drug, and Cosmetic Act or to the licensing provisions of the Public Health Service Act (58 Stat. 632, as amended (42 U.S.C. 201 et seq.)). The regulations are intended to ensure adherence to procedures and requirements governing the use of investigational new drugs, including procedures and requirements for the submission to, and review by, the Food and Drug Administration of investigational new drug applications (IND's).

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

21 USC 301 et seq.
View Law

Presidential Action:

-

Title:

Workforce Innovation and Opportunity Act (WIOA) Common Performance Reporting

Reference Number:

202509-1205-010

Omb Control Number:

1205-0526

Agency:

DOL/ETA

Received:

2025-12-02

Concluded:

2025-12-11

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Workforce Innovation and Opportunity Act (WIOA) Common Performance Reporting

Key Information

Abstract

The Workforce Innovation and Opportunity Act requires states to report on performance in core programs such as the Wagner-Peyser Act programs, the Adult, Dislocated Worker, and Youth programs, Adult Education and Family Literacy Act programs, and the Vocational Rehabilitation Act programs. This ICR contains the data to be collected for the measure states are to use to report on performance.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

29 USC 3141
View Law

Presidential Action:

-

Title:

CLIA Proficiency Testing (PT) (CMS-10690)

Reference Number:

202512-0938-002

Omb Control Number:

0938-1357

Agency:

HHS/CMS

Received:

2025-12-02

Concluded:

2026-01-28

Action:

Approved with change

Status:

Active

Request Type:

Extension without change of a currently approved collection
CLIA Proficiency Testing (PT) (CMS-10690)

Key Information

Abstract

A. Clarification for Reporting of Microbiology Organism Identification. This information is necessary to ensure that laboratories are reporting proficiency testing (PT) results for microbiology organism identification to the highest level that they report results on patient specimens. The laboratories will provide this information to the PT programs as well as CMS. B. PT Program Reapproval. This information may be needed by CMS should we require a PT program to reapply for approval using the process for initial applications if widespread or systemic problems are encountered during the reapproval process.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

Pub.L. 112 - 202 353
View Law

Presidential Action:

-

Title:

Generic Clearance for Federal Student Aid Customer Satisfaction Surveys and Focus Groups Master Plan

Reference Number:

202508-1845-008

Omb Control Number:

1845-0045

Agency:

ED/FSA

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Generic Clearance for Federal Student Aid Customer Satisfaction Surveys and Focus Groups Master Plan

Key Information

Abstract

The Higher Education Amendments of 1998 established Federal Student Aid (FSA) as the first Performance-Based Organization (PBO). One purpose of the PBO is to improve service to students and other participants in the student financial assistance programs authorized under title IV of the Higher Education Act of 1965, as amended, including making those programs more understandable to students and their parents. To do that, FSA has committed to ensuring that all people receive service that matches or exceeds the best service available in the private sector. Requirements of the legislation establish an on-going need for FSA to be engaged in an interactive process of collecting information and using it to improve program services and processes. The use of customer surveys and focus groups allows FSA to gather that information from the affected parties in a timely manner to improve communications with our product users.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Presidential Action:

-

Title:

Fees

Reference Number:

202511-3141-001

Omb Control Number:

3141-0007

Agency:

NIGC

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Fees

Key Information

Abstract

The Indian Gaming Regulatory Act (IGRA or the Act), 25 U.S.C. 2701, et seq., laid out a comprehensive framework for the regulation of gaming on Indian lands. Amongst other actions necessary to carry out the Commission’s statutory duties, the Act requires Indian tribes that conduct a class II and/or class III gaming activity to pay annual fees to the Commission on the basis of the assessable gross revenues of each gaming operation using rates established by the Commission. 25 U.S.C. 2717. The Commission is authorized to “promulgate such regulations and guidelines as it deems appropriate to implement” IGRA. 25 U.S.C. 2706(b)(10). The Commission has promulgated part 514 of title 25, Code of Federal Regulations, to implement these statutory requirements. Section 514.6 requires a tribe to submit, along with its fee payments, quarterly fee statements (worksheets) showing its assessable gross revenues for the previous fiscal year in order to support the computation of fees paid by each gaming operation. Section 514.7 requires a tribe to submit a notice within 30 days after a gaming operation changes its fiscal year. Section 514.15 allows a tribe to submit fingerprint cards to the Commission for processing by the Federal Bureau of Investigation (FBI), along with a fee to cover the NIGC’s and FBI’s cost to process the fingerprint cards on behalf of the tribes. Part of this collection is mandatory and the other part is voluntary. The required submission of the fee worksheets allows the Commission to both set and adjust fee rates, and to support the computation of fees paid by each gaming operation. In addition, the voluntary submission of fingerprint cards allows a tribe to conduct statutorily mandated background investigations on applicants for key employee and primary management official positions.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

25 USC 2701
View Law

Presidential Action:

-

Title:

Entry/Immediate Delivery Application and Simplified Entry

Reference Number:

202511-1651-004

Omb Control Number:

1651-0024

Agency:

DHS/USCBP

Received:

2025-12-01

Concluded:

2026-01-12

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Entry/Immediate Delivery Application and Simplified Entry

Key Information

Abstract

CBP Forms 3461 and 3461 Alternate are used by importers to provide CBP with the necessary information in order to examine and release imported cargo. ACE Entry filers may use the ACE Cargo Release (formerly called Simplified Entry) is a program in which importers or brokers may file Simplified Entry data in lieu of filing Form 3461.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

19 USC 1484
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Presidential Action:

-

Title:

Transfer of Cargo to a Container Station

Reference Number:

202511-1651-007

Omb Control Number:

1651-0096

Agency:

DHS/USCBP

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
Transfer of Cargo to a Container Station

Key Information

Abstract

In accordance with 19 CFR 19.42, the container station operator may make a request for the transfer of a container to the station by submitting to CBP an abstract of the manifest for the transferred containers including the bill of lading number, marks, numbers, description of the contents, and consignee.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

19 USC 1499
View Law

Presidential Action:

-

Title:

SAFECOM Nationwide Surveys Generic Clearance

Reference Number:

202511-1670-001

Omb Control Number:

1670-0048

Agency:

DHS/CISA

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
SAFECOM Nationwide Surveys Generic Clearance

Key Information

Abstract

To meet the statutory requirements of 6 U.S.C. § 573, Emergency Communications Division (ECD) is mandated to conduct the SAFECOM Nationwide Survey every 5 years to assess evolving capability needs and gaps and track progress against policy initiatives; status of strategic plans; and major industry or market shifts affecting the emergency communications capability. CISA ECD will conduct a web-based survey entitled the SAFECOM Nationwide Survey, hereinafter referred to as the SNS. The purpose of the survey is to gather information to assess available emergency communications capabilities and identify gaps and needs for emergency response providers to effectively communicate during all types of natural or man-made hazards. CISA ECD will use the information collected to complete a statutorily mandated assessment and share the data with all stakeholders that have a role in emergency communications. In order to ascertain this information, the SNS will deploy four similar surveys across the nation to various emergency response disciplines at each level of government - federal, state, territorial, tribal, and local. The survey will solicit responses regarding issues affecting the public safety community to determine a jurisdiction’s level of operability, interoperability and continuity and thus their overall emergency communications capability level. CISA ECD will analyze the data collected from this general survey to identify major gaps and themes affecting emergency communications across levels of government. Additionally, this analysis informs the development of supplemental surveys tailored to specific needs across the public safety community, as well as future iterations of the Nationwide Baseline Communications Assessment (NCBA) and National Emergency Communications Plan (NECP).

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

6 USC 571 Sec 1801
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6 USC 572 Sec 1802
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Pub.L. 109 - 295 671
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6 USC 573 Sec 1803
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Pub.L. 107 - 296 101
View Law

Presidential Action:

-

Title:

Data Collection for Quality Measures Using the Consolidated Renal Operations in a Web-Enabled Network (CROWNWeb) (CMS-10569)

Reference Number:

202512-0938-001

Omb Control Number:

0938-1289

Agency:

HHS/CMS

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Data Collection for Quality Measures Using the Consolidated Renal Operations in a Web-Enabled Network (CROWNWeb) (CMS-10569)

Key Information

Abstract

Section 1881(h) of the Social Security Act, as amended by Section 153(h) of the Medicare Improvements for Patients and Providers Act, authorizes the establishment of a quality incentive program for renal dialysis facilities. Beginning in CY 2016, renal dialysis facilities have been required to collect and submit data on quality reporting measures to CMS using Consolidated Renal Operations in a Web-Enabled Network (CROWNWeb); in CY 2018, this was increased to eight quality reporting measures. In CY 2020, we launched the End-Stage Renal Disease Quality Reporting System (EQRS), which contains the functionalities of the three legacy ESRD Systems, including CROWNWeb, in one global application, and aims to provide ongoing support to the ESRD user community to foster accurate and timely monthly data submission. The measures required for reporting under the ESRD Quality Incentive Program are designed to reflect the appropriate level of care and the most important areas of service furnished by renal dialysis facilities. Measure data are intended to be publicly reported.

Federal Register Notices

60-Day FRN
View Notice

Authorizing Statutes

42 USC 1395
View Law

Presidential Action:

-

Title:

Assessing the Fit and Comfort of Motorcycle Safety Gear

Reference Number:

202509-2127-003

Omb Control Number:

-

Agency:

DOT/NHTSA

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

New collection (Request for a new OMB Control Number)
Assessing the Fit and Comfort of Motorcycle Safety Gear

Key Information

Abstract

NHTSA seeks approval from OMB for a new information collection request to assess the fit, comfort, and preference of motorcyclists’ safety gear. The proposed study aims to address the pressing need to understand the relationship between the fit and comfort of personal protective motorcycle gear and the decision to use gear. This information collection will be a one-time voluntary collection involving assessments of motorcycle safety gear (i.e., footwear, gloves, helmets, jackets, and pants). In 2022, there were 6,218 motorcyclists killed in traffic crashes, comprising 15 percent of all traffic fatalities and 19 percent of all motor vehicle occupant (driver and passenger) fatalities, representing a fatality rate per vehicle miles traveled nearly 22 times that of passenger car occupants. These findings demonstrate the inherent risk of motorcycle riding and highlight the importance of wearing personal protective gear. Nonetheless, not all motorcyclists use gear on every ride. There are many reasons why a motorcycle rider may not wear protective gear, such as a sense of “personal freedom,” “It’s more fun to ride without a helmet,” skepticism about the protective value of helmets, and the discomfort of wearing a helmet. Even when protective gear is worn, ill-fitting gear or improperly worn gear could compromise protection. NHTSA provides specific information on its website about finding the right fit and identifying unsafe helmets, but the extent to which motorcyclists wear helmets that fit and are worn safely is unknown. Additionally, the requirements for an effective fit may vary by the type of motorcycle, riding style, and riding positions. To encourage greater and proper usage of protective gear, it is crucial to understand the factors contributing to non-adherence to safety recommendations. NHTSA is conducting this study to investigate riders' beliefs, attitudes, and perceptions regarding gear fit and comfort, and to assess the fit and comfort of gear in use. The study plans to screen 1,250 riders to reach the targeted 625 study participants with an equal number of riders of standard, cruiser, sport and adventure/touring motorcycles, and seated motor scooters; gather information about the protective gear the riders use; and assess the fit and comfort of the gear. Participation will be voluntary and anonymous. Participants will be recruited at locations where riders gather such as rallies, and other organized social or training events. Study staff will observe gear worn by riders, assess the fit of one type of protective gear (i.e., footwear, gloves, helmet, jacket, or pants) per participant, and ask riders for their opinions about the fit and comfort of the protective gear type of interest (one type of gear per participant). Additionally, study staff will use a tablet to show participants a series of images of examples of the protective gear type of interest that range in protective value (e.g., half helmet, full-face helmet); the examples will include a description of the item (e.g., composition material, ventilation/waterproof features) but not the brand name. Participants will rate each example in terms of its perceived protection and the likelihood they would use or purchase it. The intention of this collection is to learn about the experiences and perceptions of riders regarding protective gear. The collected information will inform NHTSA’s development of programs as it looks for ways to improve rider safety while still prioritizing rider comfort to ensure riding remains an enjoyable experience. NHTSA will use the collected information to produce a technical report with aggregate (summary) statistics and tables only; no personally identifiable information will be retained or reported. The technical report will be distributed to audiences interested in improving highway safety.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

23 USC 403
View Law

Presidential Action:

-

Title:

Entry Summary

Reference Number:

202511-1651-003

Omb Control Number:

1651-0022

Agency:

DHS/USCBP

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Entry Summary

Key Information

Abstract

CBP Form 7501, Entry Summary, is used to identify merchandise entering the commerce of the United States, and to document the amount of duty and/or tax paid. CBP Form 7501 is submitted by the importer, or the importer’s agent, for each import transaction. The data on this form is used by CBP as a record of the import transaction; to collect the proper duty, taxes, certifications and enforcement information; and to provide data to the U.S. Census Bureau for statistical purposes. CBP Form 7501 must be filed within 10 working days from the time of entry of merchandise into the United States. Collection of the data on this form is authorized by 19 U.S.C. 1484 and provided for by 19 CFR 142.11 and CFR 141.61. CBP Form 7501 and accompanying instructions can be found at https://www.cbp.gov/newsroom/publications/forms?title=7501&=Apply

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

19 USC 1484
View Law

Presidential Action:

-

Title:

New Animal Drug Applications; Abbreviated New Animal Drug Applications; and Veterinary Master Files

Reference Number:

202512-0910-001

Omb Control Number:

0910-0032

Agency:

HHS/FDA

Received:

2025-12-01

Concluded:

2026-01-12

Action:

Approved with change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
New Animal Drug Applications; Abbreviated New Animal Drug Applications; and Veterinary Master Files

Key Information

Abstract

FDA is requesting to include abbreviated new animal drug application information collection activity into the collection for efficiency of agency operations and because activities are conducted under related statutory authorities.

Federal Register Notices

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

Authorizing Statutes

21 USC 512
View Law

Presidential Action:

-

Title:

Minimum Technical Standards for Class II Gaming Systems and Equipment

Reference Number:

202511-3141-005

Omb Control Number:

3141-0014

Agency:

NIGC

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Minimum Technical Standards for Class II Gaming Systems and Equipment

Key Information

Abstract

The Indian Gaming Regulatory Act (IGRA or the Act), 25 U.S.C. 2701, et seq., laid out a comprehensive framework for the regulation of gaming on Indian lands. Amongst other actions necessary to carry out the Commission’s statutory duties, the Act directs the Commission to monitor class II gaming conducted on Indian lands on a continuing basis in order to ensure that the Indian tribe is the primary beneficiary of the gaming operation and to protect such gaming as a means of generating tribal revenue, and to assure that gaming is conducted fairly and honestly by both the operator and players. 25 U.S.C. 2702(2), 2706(b)(1). The Act allows Indian tribes to use “electronic, computer, or other technologic aids” to conduct class II gaming activities. 25 U.S.C. 2703(7)(A). The Commission has promulgated part 547 of title 25, Code of Federal Regulations, to aid it in monitoring class II gaming facilities that use electronic, computer, or other technologic aids to conduct class II gaming.

Federal Register Notices

60-Day FRN
View Notice
30-Day FRN
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Authorizing Statutes

25 USC 2701
View Law

Presidential Action:

-

Title:

510(k) Third-Party Review Program

Reference Number:

202504-0910-003

Omb Control Number:

0910-0375

Agency:

HHS/FDA

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
510(k) Third-Party Review Program

Key Information

Abstract

This ICR collects information from persons who wish to be accredited by the Agency to review certain premarket notifications. Participation in this third-party review program by accredited persons is entirely voluntary. A third party wishing to participate will submit a request for accreditation to FDA. Accredited third-party reviewers have the ability to review a manufacturer's premarket notification for selected medical devices. After reviewing a submission, the reviewer will forward a copy of the submission, along with the reviewer's documented review and recommendation to FDA. Third-party reviewers also maintain records of their reviews and a copy of the submission. The purpose of the program is: (1) to provide manufacturers of eligible devices with an alternative review process that could yield more rapid marketing clearance decisions and (2) enable FDA to target its scientific review resources at higher-risk devices while maintaining confidence in the review by third parties of low-to-moderate risk devices.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

21 USC 523
View Law

Presidential Action:

-

Title:

[NCHS] Division of Vital Statistics Proposal for Access to Restricted-Use Data for the National Center for Health Statistics

Reference Number:

202512-0920-001

Omb Control Number:

-

Agency:

HHS/CDC

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Existing collection in use without an OMB Control Number
[NCHS] Division of Vital Statistics Proposal for Access to Restricted-Use Data for the National Center for Health Statistics

Key Information

Abstract

NCHS is the Nation’s principal health statistics agency and compiles statistical information to guide actions and policies to improve the health of the U.S. population. The data systems administered by NCHS are a unique public resource for health information, a critical element of public health and health policy. Making these data available to the public upon request is an essential mission of NCHS. Since 1991, the NCHS DVS has sought to make restricted-use NCHS vital statistics data available to authorized researchers in a secure manner that protects the data from unauthorized disclosure. The DVS proposal collects information that is used by NCHS to assess and adjudicate researcher projects to determine whether access to restricted-use vital statistics data should be granted under the conditions established by the jurisdictions.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Presidential Action:

-

Title:

Suspected Unapproved Parts Notification

Reference Number:

202507-2120-006

Omb Control Number:

2120-0552

Agency:

DOT/FAA

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
Suspected Unapproved Parts Notification

Key Information

Abstract

The information collected on the FAA Form 8120-11 is reported voluntarily by manufacturers, repair stations, aircraft owner/operators, air carriers, and the general public who wish to report suspected unapproved parts to the FAA for review. The report information is received by the FAA’s Safety Hotline, and is used to determine if an unapproved part investigation is warranted. If the investigation confirms that the part is unapproved, and additional unapproved parts exists on other products, aircraft, or designs, the information is used as a basis for an aviation industry alert or notification. Alerts are used to inform industry of situations essential to the prevention of accidents. If the information had not been collected, the consequence to the aviation community would be the inability to determine whether or not unapproved parts are being offered for sale or use for installation on type-certificated products. Procedures and processes relating to the SUP program and associated reports are found in FAA Order 8120.16A, Suspected Unapproved Parts Program, and AC 21-29D, Detecting and Reporting Suspected Unapproved Parts. When unapproved parts are identified, the FAA notifies the public by published Field Notifications (FN), disseminated using Unapproved Parts Notifications (UPN), Aviation Maintenance Alerts, Airworthiness Directives (AD), entry into an issue of the Service Difficulty Reporting Summary, a Special Airworthiness Information Bulletin, a display on an Internet site, or direct mailing.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

49 USC 44701
View Law

Presidential Action:

-

Title:

Student Assistance General Provisions - Financial Assistance for Students with Intellectual Disabilities

Reference Number:

202508-1845-010

Omb Control Number:

1845-0099

Agency:

ED/FSA

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Reinstatement without change of a previously approved collection
Student Assistance General Provisions - Financial Assistance for Students with Intellectual Disabilities

Key Information

Abstract

This request is for a reinstatement of the most recently assessed record keeping burden requirements contained in the regulations at 34 CFR 668.232 and 668.233, related to the administrative requirement of the financial assistance for students with intellectual disabilities program. The information collection requirements are necessary to determine the eligibility to receive program benefits and to prevent fraud and abuse of the program funds.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

20 USC 1091
View Law

Presidential Action:

-

Title:

NFA Responsible Person Questionnaire

Reference Number:

202511-1140-004

Omb Control Number:

1140-0107

Agency:

DOJ/ATF

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
NFA Responsible Person Questionnaire

Key Information

Abstract

ATF Form 5320.23 is required for any responsible person (as defined in 27 CFR 479.11) who is part of a trust or legal entity that is applying on ATF Form 1, Application to Make and Register a Firearm, as the maker or is identified as the transferee on ATF Form 4, Application for Tax Paid Transfer and Registration of Firearm, or ATF Form 5, Application for Tax Exempt Transfer of Firearm. Forms 1, 4 and 5 are required under the National Firearms Act (NFA).

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

26 USC 5812
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26 USC 5822
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Presidential Action:

-

Title:

Events, Meetings, and Registrations

Reference Number:

202511-1910-001

Omb Control Number:

-

Agency:

DOE/DOEOA

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

New collection (Request for a new OMB Control Number)
Events, Meetings, and Registrations

Key Information

Abstract

This is a request for a new generic clearance as a means of promoting innovative solutions. This generic clearance will allow the Department of Energy (DOE) to provide a quick and efficient process to create application forms and manage registrations and scheduling for DOE-sponsored events, including workshops, conferences, and panels. Additionally, this request will enable DOE to respond to requests from people outside of the Department who want to schedule meetings with DOE senior officials. By collecting basic information, such as contact information, DOE will ensure that participants are registered accurately, events are well organized, and meetings are scheduled accordingly. These miscellaneous forms will be primarily administrative in nature, not to be used for programmatic purposes, and are necessary to ensure DOE has the information needed to meet public and agency need.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Presidential Action:

-

Title:

Indian Gaming Management Contract Provisions

Reference Number:

202511-3141-002

Omb Control Number:

3141-0004

Agency:

NIGC

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Indian Gaming Management Contract Provisions

Key Information

Abstract

The Indian Gaming Regulatory Act requires the National Indian Gaming Commission Chairman to review and approve all management contracts for the operation and management of class II and/or class III gaming activities, and to conduct background investigations of persons with direct or indirect financial interests in, and management responsibility for, management contracts. The Commission has promulgated parts 533, 535, and 537 of title 25, Code of Federal Regulations, to implement these statutory requirements.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

25 USC 2701
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Presidential Action:

-

Title:

Minimum Internal Control Standards for Class II Gaming

Reference Number:

202511-3141-003

Omb Control Number:

3141-0009

Agency:

NIGC

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Minimum Internal Control Standards for Class II Gaming

Key Information

Abstract

The Indian Gaming Regulatory Act (IGRA or the Act), 25 U.S.C. 2701, et seq., laid out a comprehensive framework for the regulation of gaming on Indian lands. Amongst other actions necessary to carry out the Commission’s statutory duties, the Act directs the Commission to monitor class II gaming conducted on Indian lands on a continuing basis in order to adequately shield Indian gaming from organized crime and other corrupting influences, to ensure that the Indian tribe is the primary beneficiary of the gaming operation, and to ensure that gaming is conducted fairly and honestly by both the operator and players. 25 U.S.C. 2702(2), 2706(b)(1). The Commission is also authorized to “promulgate such regulations and guidelines as it deems appropriate to implement” IGRA. 25 U.S.C. 2706(b)(10). The Commission has promulgated part 543 of title 25, Code of Federal Regulations, to aid it in monitoring class II gaming on a continuing basis.

Federal Register Notices

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

Authorizing Statutes

25 USC 2701
View Law

Presidential Action:

-

Title:

Facility License Notifications and Submissions

Reference Number:

202511-3141-004

Omb Control Number:

3141-0012

Agency:

NIGC

Received:

2025-12-01

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Facility License Notifications and Submissions

Key Information

Abstract

The Indian Gaming Regulatory Act (IGRA or the Act), Public Law 100–497, 25 U.S.C. 2701, et seq., was signed into law on October 17, 1988. The Act established the National Indian Gaming Commission (NIGC or Commission) and set out a comprehensive framework for the regulation of gaming on Indian lands. The Act sets standards for the regulation of Indian gaming, including the requirement that Indian tribes that conduct class II and/or class III gaming issue “a separate license … for each place, facility, or location on Indian lands at which class II [and class III] gaming is conducted,” 25 U.S.C. 2710(b)(1), (d)(1), and ensure that “the construction and maintenance of the gaming facilities, and the operation of that gaming is conducted in a manner which adequately protects the environment and public health and safety.” 25 U.S.C. 2710(b)(2)(E). The Commission is authorized to “promulgate such regulations and guidelines as it deems appropriate to implement” IGRA. 25 U.S.C. 2706(b)(10). The Commission has promulgated part 559 of title 25, Code of Federal Regulations, to implement these requirements.

Federal Register Notices

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

Authorizing Statutes

25 USC 2701
View Law

Presidential Action:

-
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