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.
Federal agencies are required to submit an ICR whenever they create, renew, or 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.
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.
Showing 20 of 704 results
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Agency
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Received
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Expires
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| 202006-0572-005 | Rural Broadband Loans, Loan/Grant Combination, and Loan Guarantees | USDA/RUS | 2020-12-08 | 2025-12-31 | Revision of a currently approved collection
Rural Broadband Loans, Loan/Grant Combination, and Loan Guarantees
Key Information
Abstract
The Rural Utilities Service (RUS), is authorized by Title VI, Rural Broadband Access, of the Rural Electrification Act of 1936, as amended (RE Act), to provide loans, loan/grant combinations and loan guarantees to fund the cost of construction, improvement, or acquisition of facilities and equipment for the provision of broadband service in eligible rural areas in the States and Territories of the United States. 7 CFR part 1738 prescribes the types of loans available, facilities financed, and eligible applicants, as well as minimum equity requirements to be considered for a loan. In addition, 7 CFR part 1738 outlines the process through which RUS will consider applicants under the priority consideration required in Title VI. |
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| 202101-0570-001 | 7 CFR 1980-E, Business and Industrial Loan Program | USDA/RBS | 2021-11-10 | 2025-12-31 | Extension without change of a currently approved collection
7 CFR 1980-E, Business and Industrial Loan Program
Key Information
Abstract
The collection of information is submitted to the Agency for use in making program eligibility, financial feasability, and loan security determinations. |
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| 202211-0575-017CF | SF 424 - Application for Federal Assistance (4040-0004) | USDA/RHS | 2022-11-08 | 2025-12-31 | RCF Recertification
SF 424 - Application for Federal Assistance (4040-0004)
Key Information
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| 201912-1405-004 | Adoption Family Relief Act Refund Application | STATE/AFA | 2019-12-31 | 2025-12-31 | Extension without change of a currently approved collection
Adoption Family Relief Act Refund Application
Key Information
Abstract
The Adoptive Family Relief Act allows for the waiver or refund certain immigrant visa fees for a lawfully adopted child. This collection will gather information to determine the extra fees these families have paid in order to refund them. |
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| 202101-1625-005 | Small Passenger Vessels -- Title 46 Subchapters K and T | DHS/USCG | 2021-02-24 | 2025-12-31 | Extension without change of a currently approved collection
Small Passenger Vessels -- Title 46 Subchapters K and T
Key Information
Abstract
The information requirements are necessary for the proper administration and enforcement of the program on safety of commercial vessels as it affects small passenger vessels. The requirements affect small passenger vessels (under 100 gross tons) that carry more than 6 passengers.. |
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| 202202-0910-019 | Current Good Manufacturing Practices for Positron Emission Tomography (PET) Drugs | HHS/FDA | 2022-10-13 | 2025-12-31 | Extension without change of a currently approved collection
Current Good Manufacturing Practices for Positron Emission Tomography (PET) Drugs
Key Information
Abstract
This information collection supports information collection requirements under the Current Good Manufacturing Practice regulations for Positron Emission Tomography (PET) drugs. The regulations establish recordkeeping requirements that include: Batch Production and Control Records; Equipment and Facilities Records; Records of Components, Containers, and Closures; Process Vertification; Laboratory Testing Records; Sterility Test Failure Notices; Conditional Final Releases; Out-of-Specification Investigations; Reprocessing Procedures; Distribution Records; and Complaints. The regulations also require 3rd Party Disclosure requirements regarding specific notices. Respondents to the collection are manufacturers of PET drugs. |
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| 202210-3045-002 | AmeriCorps State and National Project Progress Reports (PPRs) | CNCS | 2022-10-31 | 2025-12-31 | Revision of a currently approved collection
AmeriCorps State and National Project Progress Reports (PPRs)
Key Information
Abstract
The Corporation for National and Community Service requires grantees of its AmeriCorps State and National program to submit Project Progress Reports (PPRs). This information Collection comprises the questions that these grantees will answer to report their progress to the agency. This revision includes two new questions to the PPRs to address new cross-government initiatives and better understand how many beneficiaries in poverty are being served. |
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| 202205-0704-003 | Post-Election Voting Survey of State Election Officials (SEOs) | DOD/DODDEP | 2022-10-17 | 2025-12-31 | Existing collection in use without an OMB Control Number
Post-Election Voting Survey of State Election Officials (SEOs)
Key Information
Abstract
To gather feedback from the state election officials (SEOs) responsible for administering UOCAVA on behalf of the military and overseas voters. This survey will help FVAP understand how it can best engage election officials and identify areas where its processes can be improved. |
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| 202212-7100-007 | Savings Association Holding Company Report | FRS | 2022-12-20 | 2025-12-31 | Extension without change of a currently approved collection
Savings Association Holding Company Report
Key Information
Abstract
The FR LL-(b)11 collects from certain savings and loan holding companies (SLHCs) information about their Securities and Exchange Commission (SEC) filings, reports, financial statements, and other exhibits that the Board requires. The Board uses this data to analyze the financial condition of respondent SLHCs and assess regulatory compliance. |
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| 202301-2070-003 | Pesticides Data Call In Program (Non-Substantive Change) | EPA/OCSPP | 2023-02-13 | 2025-12-31 | No material or nonsubstantive change to a currently approved collection
Pesticides Data Call In Program (Non-Substantive Change)
Key Information
Abstract
This ICR covers the information collection activities associated with the issuance of DCIs under section 3(c)(2)(B) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA). EPA regulates the use of pesticides under the authority of two federal statutes: FIFRA (7.U.S.C. 136 et seq.) and the Federal Food, Drug and Cosmetic Act (FFDCA) (21 U.S.C. 346). In general, before manufacturers can sell pesticides in the United States, EPA must evaluate the pesticides thoroughly to ensure that they meet federal safety standards to protect human health and the environment. EPA grants a "registration" or license that permits a pesticide's distribution, sale, and use only after the company meets the scientific and regulatory requirements. In evaluating a pesticide registration application, EPA assesses a wide variety of potential human health and environmental effects associated with the use of the product. Applicants, or potential registrants, must generate or provide the scientific data necessary to address concerns pertaining to the identity, composition, potential adverse effects, and environmental fate of each pesticide. The data allow EPA to evaluate if a pesticide has the potential to cause harmful effects on certain non-target organisms and endangered species, and on surface or ground water. Through a scientific and public process, EPA specifies the kinds of data and information necessary to make regulatory judgments about the risks and benefits of pesticide products under FIFRA sections 3, 4 and 5, as well as the data and information needed to determine the safety of pesticide chemical residues under FFDCA section 408. The regulations in 40 CFR part 158 describe the minimum data and information EPA typically requires in an application for pesticide registration or amendment; reregistration of a pesticide product; maintenance of a pesticide registration by means of the DCI process (e.g., as used in the registration review program); or to establish or maintain a tolerance or exemption from the requirements of a tolerance for a pesticide chemical residue. EPA uses the DCIs issued under this ICR to acquire the data necessary for its statutorily mandated review of a pesticide’s registration, which assess if the continued registration of a pesticide causes an unreasonable adverse effect on human health or the environment. |
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| 202211-0581-001CF | 4040-0004 Application for Federal Assistance SF-424 | USDA/AMS | 2022-11-08 | 2025-12-31 | RCF Recertification
4040-0004 Application for Federal Assistance SF-424
Key Information
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| 202410-0910-010 | Warning Plans for Smokeless Tobacco Products | HHS/FDA | 2024-10-25 | 2025-12-31 | No material or nonsubstantive change to a currently approved collection
Warning Plans for Smokeless Tobacco Products
Key Information
Abstract
Section 3 of the Comprehensive Smokeless Tobacco Health Education Act of 1986 (the Smokeless Tobacco Act), requires, among other things, that all smokeless tobacco product packages and advertisements bear one of four required warning statements. This information collection--the submission to FDA of warning plans for smokeless tobacco products--is statutorily mandated. Section (b)(3)(A) of 15 U.S.C. 4402 requires that the warnings be displayed on packaging and advertising for each brand of smokeless tobacco “in accordance with a plan submitted by the tobacco product manufacturer, importer, distributor, or retailer” to, and approved by, FDA. The warning plans will be reviewed by FDA to determine whether the companies' plans for the equal distribution and display of warning statements on packaging and the quarterly rotation of warning statements in advertising for each brand requires, among other things, that all smokeless tobacco product packages and advertisements bear one of four required warning statements. |
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| 202205-0920-009 | Requirement for Airlines and Operators to Collect and Transmit Designated Information for Passengers and Crew Arriving Into the United States | HHS/CDC | 2022-05-26 | 2025-12-31 | Extension without change of a currently approved collection
Requirement for Airlines and Operators to Collect and Transmit Designated Information for Passengers and Crew Arriving Into the United States
Key Information
Abstract
In order to control the introduction, transmission, and spread of communicable diseases, such as COVID-19, into the United States, the collection of traveler contact information helps ensure that CDC and state and local health authorities are able to identify and locate persons arriving in, or transmitting through, the United States from a foreign country who may have been exposed to a communicable disease abroad. State, local, and territorial public health departments can use this information to connect with travelers who arrive in their jurisdictions infectious with or exposed to a communicable disease in order to monitor travelers for symptoms as needed. This Extension ICR is submitted to permit the continued collection of data from travelers to effectively make and enforce regulations necessary to prevent the spread of communicable diseases in the United States. |
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| 202206-0694-005 | License Exemptions and Exclusions | DOC/BIS | 2022-10-26 | 2025-12-31 | Extension without change of a currently approved collection
License Exemptions and Exclusions
Key Information
Abstract
Over the years, BIS has worked with other Government agencies and the affected public to identify areas where export licensing requirements may be relaxed without jeopardizing U.S. national security or foreign policy. Many of these relaxations have taken the form of licensing exceptions and exclusions. Some of these license exceptions and exclusions have a reporting or recordkeeping requirement to enable the Government to continue to monitor exports of these items. Exporters may choose to utilize the license exception and accept the reporting or recordkeeping burden in lieu of submitting a license application. These exceptions and exclusions have allowed exporters to ship items quickly, without having to wait for license approval. |
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| 202203-0910-007 | Postmarket Surveillance of Medical Devices | HHS/FDA | 2022-11-22 | 2025-12-31 | Extension without change of a currently approved collection
Postmarket Surveillance of Medical Devices
Key Information
Abstract
This information collection implements section 522 of the Federal Food, Drug, and Cosmetic Act, which governs the postmarket surveillance of medical devices. Respondents to the information collection are medical device manufacturers who must conduct surveillance in accordance with statutory orders issued by FDA in support of the clearance or approval of certain devices. The information collection is intended to ensure the continued safety of medical devices. |
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| 202211-2900-001CF | SF-424 Application for Federal Assistance | VA | 2022-11-08 | 2025-12-31 | RCF Recertification
SF-424 Application for Federal Assistance
Key Information
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| 202207-0584-003 | SNAP Employment and Training Performance Measurement, Monitoring and Reporting Requirements | USDA/FNS | 2022-11-22 | 2025-12-31 | Revision of a currently approved collection
SNAP Employment and Training Performance Measurement, Monitoring and Reporting Requirements
Key Information
Abstract
In accordance with Section 16(h)(5) of the Food and Nutrition Act (FNA), as amended by section 4022 of the Agriculture Act of 2014, and 7 CFR 273.7(c)(17) the Department requires that State agencies report outcome data for the Supplemental Nutrition Employment Program (SNAP) Employment and Training (E&T) programs. In order for FNS to monitor the effectiveness of E&T programs State agencies are required to report outcome data on five separate reporting measures: (1) the number and percentage of E&T participants who retain employment 2 quarters and 4 quarters after completing E&T (2) the median wages for participants with earnings 2 quarters after completion of E&T (3) the number and percentage of participants that completed a training, education, work experience or on-the-job training component; (4) certain unique characteristics of SNAP E&T participants; and (5) additional reporting requirements for State agencies that pledge to serve all at-risk Able-bodied Adults without Dependents (ABAWDs). State agencies are also required to identify appropriate reporting measures for each proposed component that serves a threshold number of participants of at least 100 a year. State agencies identify the reporting measures for these components in State agencies’ E&T plans and report the outcome data to the Food and Nutrition Service (FNS) through State agencies’ annual reports. State agencies are required to report outcome data annually. |
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| 202211-0910-012 | Establishment, Maintenance, and Availability of Records; Additional Traceability Records for Certain Foods | HHS/FDA | 2022-12-05 | 2025-12-31 | Revision of a currently approved collection
Establishment, Maintenance, and Availability of Records; Additional Traceability Records for Certain Foods
Key Information
Abstract
This information collection request supports agency rulemaking to establish additional recordkeeping requirements pertaining to the traceability of foods. Respondents to the information collection are persons who manufacture, process, pack, or hold foods. |
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| 202211-0930-002 | Notification of Intent to Use Schedule III, IV, or V Opioid Drugs for the Maintenance and Detoxification Treatment of Opiate Addiction | HHS/SAMHSA | 2022-11-08 | 2025-12-31 | Extension without change of a currently approved collection
Notification of Intent to Use Schedule III, IV, or V Opioid Drugs for the Maintenance and Detoxification Treatment of Opiate Addiction
Key Information
Abstract
The Drug Addiction Treatment Act of 2000 establishes conditions for physicians to obtain waivers to permit them to prescribe certain approved narcotic treatment medications for the maintenance or detoxification treatment of opioid addiction. Under the SUPPORT Act, this data collection will include other practitioners who meet the statutory requirements: nurse practitioners, physician assistants, nurse specialist, nurse-midwives, and registered nurse anesthetists. SAMHSA will adding three additional forms from OMB No. 0930-0369. |
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| 202210-1210-002 | Plan Asset Transactions Determined by In-House Asset Managers under Prohibited Transaction Class Exemption 96-23 | DOL/EBSA | 2022-12-14 | 2026-01-31 | Extension without change of a currently approved collection
Plan Asset Transactions Determined by In-House Asset Managers under Prohibited Transaction Class Exemption 96-23
Key Information
Abstract
The Department of Labor (the Department) has the authority, pursuant to section 408(a) of the Employee Retirement Income Security Act of 1974 (ERISA) and section 4975(c)(2) of the Internal Revenue Code of 1986 (the Code), to grant an exemption from all or part of the restrictions imposed, respectively, by sections 406 and 407(a) of ERISA and from taxes imposed by sections 4975(a) and (b) of the Code by reason of section 4975(c)(1)(A) through (F) of the Code. On April 10, 1996, the Department granted PTE 96-23 (61 FR 15975-01), Class Exemption for Plan Asset Transactions Determined by In-House Asset Managers. The class exemption permits various parties in interest to employee benefit plans to engage in transactions involving plan assets if, among other requirements, the assets are managed by an in-house asset manager (INHAM). The amendment to PTE 96-23, among other things, broadens the definition of INHAM to permit a greater number of entities to take advantage of the relief provided by the exemption, proposes relief for entities that are parties in interest because they are |
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