Change Requests

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Air Bag Deactivation

Key Information

Abstract

This information collection request (ICR) is to request reinstatement with modification of a previously approved information collection associated with the process of obtaining authorization for the installation of retrofit air bag switches. Specifically, the National Highway Traffic Safety Administration (NHTSA) is requesting reinstatement of the ICR with OMB Control No. 2127-0588. 49 CFR part 595, subpart B, establishes the conditions that make it possible for vehicle owners to have their motor vehicles retrofitted with air bag switches by motor vehicle dealers and repair businesses if the owners are, or a user of their vehicle is, a member of one of the enumerated risk groups. This ICR contains two forms: the Request Form for Frontal Air Bag On-Off Switch (“Request Form”) and the Installation of Air Bag On-Off Switch Form (“Installation Form”). The Request Form corresponds to Appendix B of Part 595, which an owner or lessee of a motor vehicle seeking the installation of a retrofit air bag on-off switch must complete and submit to NHTSA. NHTSA will review and grant or deny the request for an air bag switch to be installed. The Installation Form corresponds to Appendix C of Part 595, Subpart B which air bag switch installers must return to NHTSA upon completion of an air bag switch installation. This second form was not included in the previously approved ICR. NHTSA estimates this collection will impact 300 respondents each year and will have a total annual burden of 90 hours and annual labor cost of $1,785.00.

Federal Register Notices

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

Authorizing Statutes

49 USC 30101	View Law

49 USC 30122	View Law

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Railroad Noise Emission Compliance Regulations

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Abstract

Under authority granted by the Noise Control Act of 1972, the Environmental Protection Agency (EPA) has established limits for noise emissions related to rail carriers in 40 CFR part 201. Those limits are enforced by FRA under 49 CFR part 210. In particular, the information FRA collects under § 210.27 is necessary to ensure compliance with EPA noise standards for new locomotives.This information collection is mandatory and submitted as needed.

Federal Register Notices

60-Day FRN	View Notice

Authorizing Statutes

42 USC 4916	View Law

42 USC 4905	View Law

Pub.L. 117 - 58 22423	View Law

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OVC TTAC Feedback form package

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Abstract

This collection would obtain information from OVC technical assistance recipients about their satisfaction with the assistance, their perception of the usefulness of the assistance, and their feedback about how such assistance can be improved. This information will be used by OVC for monitoring how well the assistance meets the needs of the victim services field, and for improving such assistance. This action will combine 2 previously approved collections (1121-0336 and 1121-0342) together with 1121-0341 to collect similar information.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 98 - 473 10601	View Law

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Law Enforcement Public Contact Data Collection

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Abstract

Under 34 USC § 41303 & 28 USC § 534, the FBI UCR Program will begin collecting data on law enforcement contacts with the public to provide additional context to the National Use-of-Force Data Collection. This collection is needed to collect the number of contacts law enforcement officers have with the public in three major categories; citizen calls for service, unit/officer-initiated contacts, and court/bailiff activities.

Federal Register Notices

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

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Application for Immigrant Visa and Alien Registration

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Department of State consular officers use the DS-260, in conjunction with a personal interview, to elicit information necessary to fulfill the legal requirements for the issuance of an immigrant visa. The information required on the form is necessary for consular officer to determine the eligibility and classification of an individual seeking an immigrant visa to the United States.

Federal Register Notices

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

Authorizing Statutes

8 USC 1201	View Law

8 USC 1202	View Law

8 USC 1182	View Law

8 USC 1158	View Law

8 USC 1101	View Law

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Semi-Annual Progress Report for Technical Assistance Program

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Abstract

The semi-annual progress report will be completed by all technical assistance providers receiving funds under the Office on Violence Against Women's (OVW)Technical Assistance (TA) Program. The primary purpose of the OVW Technical Assistance Program is to provide direct assistance to grantees and their subgrantees to enhance the success of local projects they are implementing with Violence Against Women Act grant funds. In addition, OVW is focused on building the capacity of criminal justice and victim services organizations to respond effectively to sexual assault, domestic violence, dating violence, and stalking and to foster partnerships between organizations that have not traditionally worked together to address violence against women, such as faith- and community- based organizations.

Federal Register Notices

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

Authorizing Statutes

34 USC 12291(b)(11)	View Law

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FORM 14: ELECTRONIC SUBMISSION OF ALLEGATIONS AND DISCLOSURES

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OSC Form 14 is used by current and former federal employees and applicants for federal employment, and other covered filers, to submit allegations of possible prohibited personnel practices or other prohibited activities for investigation and possible prosecution by OSC, or review and possible referral to relevant inspector general offices.

Federal Register Notices

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

Authorizing Statutes

5 USC CFR 1800	View Law

5 USC 1212	View Law

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Information Collection to provide for the amount of AqueousFilm Forming Foam (AFFF) located at Part 139 airports

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Abstract

In accordance with the Paperwork Reduction Act of 1995, FAA invites public comments about our intention to request the Office of Management and Budget (OMB) approval for an information collection. The collection involves S.4319 - A bill to provide for progress reports on the national transition plan related to a fluorine-free firefighting foam that requires that the FAA provide progress reports on the status of Part 139 airports transition to fluorine-free firefighting foam no later than 180 days after the date of enactment of this Act, and every 180 days thereafter until the progress report termination date. Within this report, a comprehensive list of the amount of AFFF at each part 139 airport has as of the date of the submission of the progress report, including the amount of such firefighting foam held in firefighting equipment and the number of gallons regularly kept in reserve at each such airport. These progress reports on the development and implementation of a national transition plan related to a fluorine-free firefighting foam that meets the performance standards referenced in Chapter 3 – Agent Compatibility, Substitutions, and Performance Requirements of Advisory Circular 150/5210.6E – Aircraft Fire Extinguishing Agents for Airports (AC 150/5210.62) issued on November 27, 2023 shall be submitted to the appropriate committees of Congress.

Federal Register Notices

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

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Exchange Act Form 10-K

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Section 13(a) of the Securities Exchange Act of 1934 (“Exchange Act”) requires every issuer with a class of securities registered pursuant to Section 12 of the Exchange Act to file periodic and current reports with the Commission. Section 15(d) of the Exchange Act requires each issuer with an effective registration statement under the Securities Act of 1933 to file periodic reports and documents pursuant to Section 13 of the Exchange Act. Issuers use Form 10-K (17 CFR 249.310) to satisfy their annual reporting obligations pursuant to Section 13 or 15(d) of the Exchange Act. Form 10-K requires financial and certain other information about the issuer.

Federal Register Notices

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

Authorizing Statutes

15 USC 78m, 78o(d)	View Law

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Request for Individual Access to Records Protected Under the Privacy Act

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Abstract

The Creating Advanced Streamlined Electronic Services for Constituents Act of 2019 (CASES Act), Pub. L. 116-50, 133 Stat. 1073 (2019), requires Federal agencies to establish a digital process for identity-proofed and authenticated individuals to request access to their records protected by the Privacy Act of 1974 (Privacy Act) (5 U.S.C. 552a of the United States Code). To comply with the CASES Act and OMB Memorandum, M 21-04, and pursuant to authority under sections 702(a)(5) and 1106(a) of the Social Security Act (42 U.S.C. 902(a)(5), 1306(a)), the Social Security Administration (SSA) developed Form SSA-2288-OP1, Request for Individual Access to Records Protected Under the Privacy Act, a dynamic webform that guides respondents through the information necessary to submit an electronic request for access to agency records about themselves. Under SSA’s regulations at 20 CFR 401.40 regarding individuals’ access rights under the Privacy Act (5 U.S.C. 552a(f)), individuals may request access to their records by visiting their local Social Security field office or writing to the manager of the applicable system of records. Since SSA currently has no special agency form available to the public to submit this type of request, we are implementing Form SSA-2288-OP1 to comply with the CASES Act, the Privacy Act, OMB M 21-04, and SSA’s governing regulations at 20 CFR 401.30 - 401.95. Form SSA-2288-OP1 is an electronic webform that respondents submit online only via SSA’s Upload Documents portal (OMB No. 0960-0830), after the portal first appropriately identity-proofs and authenticates respondents, consistent with requirements in the CASES Act and OMB M 21-04. Respondents can use Form SSA-2288-OP1 to request access to records or information about themselves from SSA’s program files. Pursuant to the Privacy Act and SSA’s regulations, a special procedure governs access requests that include medical records (5 U.S.C. 552a(f)(3) and 20 CFR 401.55). Therefore, respondents requesting medical record requests via Form SSA-2288-OP1 must designate an individual (such as a health professional or other responsible individual) to receive and review the records and inform the respondent of its contents. SSA may grant the respondent direct access to their medical records if it determines direct access is not likely to have an adverse effect on the respondent. Respondents who cannot (or do not wish to) submit their request electronically or seek other types of records can always avail themselves of SSA’s existing service delivery channels, such as visiting or calling their local Social Security office, or submitting a written request by mail, fax, or hand delivery. Respondents can learn more about SSA’s privacy program from its privacy webpage at www.ssa.gov/privacy, which contains sub-pages with additional information about Privacy Act requests and a link to Form SSA-2288-OP1. Respondents may also find Form SSA-2288-OP1 within the Upload Documents portal, or on SSA’s Forms webpage at www.ssa.gov/forms. Respondents are the subjects of the record(s) protected by the Privacy Act, who request access to agency records about themselves.

Federal Register Notices

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

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Regulation O

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The Federal Trade Commission requests clearance for its shared enforcement authority with the Consumer Financial Protection Bureau for the disclosure requirements contained in the CFPB's Regulation O.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 111 - 8 626(a)	View Law

12 USC 5581	View Law

Pub.L. 111 - 24 511	View Law

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Identification of Explosive Materials

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To protect the public from misuse of explosives, implementing regulations at 27 CFR 555.109 require licensees/permittees to mark certain explosives they manufacture or import, as well as mark immediate containers and outside packaging. The markings must include certain information and be clear and permanent, though they can be done via sticky label, marker, etc. Some types of explosives are too small or too fluid, in a form that cannot be marked, and are excepted.

Federal Register Notices

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

Authorizing Statutes

18 USC 923	View Law

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Approval of Laboratories for Conducting Aquatic Animal Tests for Export Health Certificates

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The purpose of this information collection is to provide approval to laboratories to conduct tests for the export of aquatic animals. The information collection activities permit APHIS to vet the laboratories.

Federal Register Notices

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

Authorizing Statutes

7 USC 8301	View Law

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Data Request and Attestation for PDP Sponsors (CMS-10691)

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42 CFR 423.513(g)(1)(i) states that beginning in plan year 2020, a PDP sponsor may submit a request to CMS for the data described in paragraph (g)(2) about enrollees in its prescription drug plans. In addition, paragraph (g)(5) provides that as a condition of receiving the requested data, the PDP sponsor must attest that it will adhere to the permitted uses and limitations on the use of the Medicare claims data listed in paragraphs (g)(3) and (4).

Federal Register Notices

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

Authorizing Statutes

Pub.L. 115 - 123 50354	View Law

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Petition for a Nonimmigrant Worker

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Abstract

USCIS uses Form I-129 and accompanying supplements to determine whether the petitioner and foreign national beneficiary(ies) is (are) eligible for the nonimmigrant classification. A U.S. employer, or agent in some instances, may file a petition for nonimmigrant worker to employ foreign nationals under the following nonimmigrant classifications: H-1B, H-2A, H-2B, H-3, L-1, O-1, O-2, P-1, P-2, P-3, P-1S, P-2S, P-3S, Q-1, or R-1 nonimmigrant worker. The collection of this information is also required from a U.S. employer on a petition for an extension of stay or change of status for E-1, E-2, E-3, Free Trade H-1B1 Chile/Singapore nonimmigrants and TN (NAFTA workers) who are in the United States. The non-substantial change is adding the electronic filing option.

Federal Register Notices

60-Day FRN	View Notice

Authorizing Statutes

8 USC 1101	View Law

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Medicare Current Beneficiary Survey (MCBS) (CMS-P-0015A)

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Abstract

The Medicare Current Beneficiary Survey (MCBS) is a continuous, multipurpose survey of a nationally representative sample of aged, disabled, and institutionalized Medicare beneficiaries. MCBS, which is sponsored by the Centers for Medicare & Medicaid Services (CMS), is the only comprehensive source of information on the health status, health care use and expenditures, health insurance coverage, and socioeconomic and demographic characteristics of the entire spectrum of Medicare beneficiaries. The MCBS has been at the forefront of survey collection and data processing, most notably as one of the first surveys to successfully 1) implement a computer assisted personal interview (CAPI) and 2) match survey and claims data to adjust and correct for underreporting in survey reported health care utilization. The CMS vision for the MCBS is to continue to provide timely, policy-relevant, unique, high-quality, and high-value data; increase the survey’s ability to develop, monitor, assess, and evaluate the impact of CMS care delivery and payment models; and to continue to break ground in innovative, efficient, and analytically powerful new areas of survey data administration, design, and development. CMS routinely reviews MCBS content to: 1) promote efficiency by streamlining the questionnaire and reducing respondent burden; 2) assess utility of information collected by the MCBS and remove questions that are no longer relevant, and 3) maintain the production of high-quality data by removing content that is no longer performing well. Starting with the 2026 full clearance revisions (approved by OMB on 1/6/2026), CMS reduced MCBS respondent burden by 8%. In accordance with OMB’s terms of clearance specified in the approval of the 2026 MCBS, CMS identified additional deletions in the Community and Facility instruments to reduce the respondent burden associated with the MCBS. When implemented, the revision to this OMB package will continue the downward trend in respondent burden with a net decrease of an additional one percent.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 108 - 173 723	View Law

Pub.L. 111 - 148 3021	View Law

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Establishing That a Tobacco Product Was Commercially Marketed in the United States As of February 15, 2007

Key Information

Abstract

The guidance document provides information on how a manufacturer may establish that a tobacco product was commercially marketed in the United States as of February 15, 2007. A "Pre-Existing" tobacco product is not considered a new tobacco product and thus is not subject to the premarket requirements of the FD&C Act. A Pre-Existing tobacco product may also serve as the predicate tobacco product in a section 905(j) report (intended to be used toward demonstrating substantial equivalence) for a new tobacco product (section 905(j)(1)A)(i) of the FD&C Act( 21 U.S.C. 387e(j)(1)(A)(i))). FDA interprets the phrase "as of February 15, 2007," as meaning that the tobacco product was commercially marketed in the United States on February 15, 2007. The guidance associated with this collection of information recommends that the manufacturer submit information adequate to demonstrate that the tobacco product was commercially marketed in the United States as of February 15, 2007. Examples of such information may include, but are not limited to, the following: dated copies of advertisements, dated catalog pages, dated promotional material, and dated bills of lading.

Federal Register Notices

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

Authorizing Statutes

21 USC 387	View Law

Pub.L. 111 - 111 31	View Law

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Consumer Assessment of Healthcare Providers and Systems (CAHPS) Survey for the Merit-Based Incentive Payment System (MIPS) (CMS-10450)

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Abstract

Section 1848(q) of the Social Security Act, as amended by section 101 of the Medicare Access and CHIP Reauthorization Act of 2015, authorizes the establishment of a Merit-based Incentive Payment System (MIPS) for eligible clinicians. Beginning in CY 2017, eligible clinicians are required to collect and submit data on four performance categories to CMS (quality, cost, advancing care information and improvement activities). This program replaces and consolidates portions of the PQRS, Value-based Modifier, and the Medicare EHR Incentive Program. The Act also establishes a second track, Advanced Alternative Payment Models (APMs) for clinicians to participate in instead of MIPS. The CAHPS survey information is used for quality reporting to collect data on fee-for-service Medicare beneficiaries’ experiences of care with eligible clinicians participating in MIPS, the Physician Compare website, and annual statistical reports describing MIPS data for all MIPS eligible clinicians.

SPD-15 Implementation	Yes

Federal Register Notices

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

Authorizing Statutes

Pub.L. 111 - 148 10331	View Law

42 USC 1395w-4	View Law

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Medicare and Medicaid Programs: Conditions of Participation for Portable X-ray Suppliers (CMS-R-43)

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Abstract

The information is required to certify portable X-ray suppliers wishing to participate in the Medicare program. The information collection is needed to determine if portable X-ray suppliers are in compliance with published health and safety requirements. This is standard medical practice and is necessary in order to ensure the well-being and safety of patients and professional treatment accountability.

Federal Register Notices

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

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Information Furnishers Rule

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Abstract

The Federal Trade Commission requests renewed clearance of the information collection provisions associated with its Information Furnishers Rule which implements section 312 of the Fair and Accurate Credit Transactions Act of 2003 and Title X of the Dodd-Frank Wall Street Reform and Consumer Protection Act and its shared enforcement of the CFPB's Regulation V (Subpart E).

Federal Register Notices

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

Authorizing Statutes

Pub.L. 108 - 159 312	View Law

Pub.L. 111 - 203 1029	View Law

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Animal Welfare

Key Information

Abstract

The records and reports herein provide APHIS with the data necessary for the review and evaluation of program compliance by regulated facilities, and provide a workable enforcement system to carry out the requirements of the Animal Welfare Act (AWA).

Federal Register Notices

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

Authorizing Statutes

7 USC 2131	View Law

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Tobacco Products, Exemptions From Substantial Equivalence Requirements

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Abstract

FDA has established in its regulations a pathway for manufacturers to request exemptions from the substantial equivalence requirements of the FD&C Act. An exemption request must be submitted with supporting documentation, the manufacturer's contact information, and a detailed explanation of the modification and its purpose. This information is submitted to FDA so FDA can determine whether an exemption from substantial equivalence to the predicate product is appropriate for the protection of the public health. FDA determines whether to grant or deny the request for an exemption based on whether the criteria in the statute have been satisfied. If FDA determines that the information is insufficient, FDA may request additional information from the manufacturer. If the manufacturer fails to respond within the timeframe requested, FDA will consider the exemption request withdrawn. FDA may rescind an exemption where necessary to protect the public health. FDA may exempt tobacco products that are modified by adding or deleting a tobacco additive, or increasing or decreasing the quantity of an existing tobacco additive, from the requirement of demonstrating substantial equivalence if the Agency determines that (1) the modification would be a minor modification of a tobacco product, (2) a report demonstrating substantial equivalence is not necessary for the protection of public health, and (3) an exemption is otherwise appropriate.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 111 - 111 31	View Law

21 USC 387e	View Law

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Request Type:

The USMCA Automotive Rules of Origin Motor Vehicle Producer Questionnaire

Key Information

Abstract

The United States International Trade Commission (Commission) is conducting a factfinding investigation (Inv. No. 332-608) to analyze the impacts of the automotive rules of origin (ROOs) in the United States-Mexico-Canada Agreement (USMCA), including their impact on the U.S. economy, effects on the competitiveness of the U.S. automotive industry, and the relevancy of the ROOs in light of technological changes. This investigation is in connection with United States-Mexico-Canada Agreement Implementation Act (19 U.S.C. 4532(g)(2)) (“the Act”). The Act requires the Commission to prepare a series of five biennial reports on the USMCA automotive ROOs, and to provide those reports to the President, the House Committee on Ways and Means, and the Senate Committee on Finance. The first of the reports was delivered on June 30, 2023, and the second was delivered on July 1, 2025. There are three additional reports due in 2027, 2029, and 2031. Similar to the second report, the Commission is conducting a survey of motor vehicle producers with U.S. production operations for the 2027 report and will deliver the results of its investigation by July 1, 2027.

Federal Register Notices

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

Authorizing Statutes

19 USC 1332	View Law

19 USC 4532(g)(2)	View Law

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Farm Loan Programs - Direct Loan Servicing - Regular

Key Information

Abstract

Information is used to determine borrower compliance with loan covenants, assist borrower in achieving their business goals, and regular servicing of loan account such as graduation, subordination, partial release, and use of proceeds.

Federal Register Notices

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

Authorizing Statutes

7 USC 1921	View Law

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Expanded Food and Nutrition Education Program (EFNEP)

Key Information

Abstract

The general purpose of the Nutrition Education Evaluation and Reporting System (NEERS) is to provide the data needed to assure the quality of the educational program and to provide diagnostic assessments of participant needs and summarize data for state and national assessment of the program's impact.

SPD-15 Implementation	Yes

Federal Register Notices

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

Authorizing Statutes

Pub.L. 612 - 331 7116	View Law

Presidential Action: