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.
Showing 25 of 1349 results
Reference Number
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Title
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Agency
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Received
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Concluded
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Action
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Status
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Request Type
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Presidential Action
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OMB Control Number
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| 202508-0910-001 | Center for Devices and Radiological Health Appeals Processes | HHS/FDA | 2025-12-04 | None | None | Received in OIRA | Reinstatement without change of a previously approved collection
Center for Devices and Radiological Health Appeals Processes
Key Information
Abstract
This guidance document helps implement section 517A of the Federal Food, Drug, and Cosmetic Act ,which governs judicial review of certain actions pertaining to medical devices and decisions or actions by Center for Devices and Radiological Health (CDRH or the Center) employees. |
- | 0910-0738 | ||
| 202512-3060-006 | Advanced Methods to Target and Eliminate Unlawful Robocalls, Sixth Report and Order, CG Docket No. 17-59, Call Authentication Trust Anchor, Fifth Report and Order, WC Docket No. 17-97, FCC 22-37 | FCC | 2025-12-04 | None | None | Received in OIRA | Extension without change of a currently approved collection
Advanced Methods to Target and Eliminate Unlawful Robocalls, Sixth Report and Order, CG Docket No. 17-59, Call Authentication Trust Anchor, Fifth Report and Order, WC Docket No. 17-97, FCC 22-37
Key Information
Authorizing Statutes
Abstract
The Federal Communications Commission seeks to establish a new information collection associated with the Advanced Methods to Target and Eliminate Unlawful Robocalls Sixth Report and Order and Call Authentication Trust Anchor Fifth Report and Order (“Gateway Provider Report and Order”). Unwanted and illegal robocalls have long been the Federal Communication Commission’s (“Commission”) top source of consumer complaints and one of the Commission’s top consumer protection priorities. Foreign-originated robocalls represent a significant portion of illegal robocalls, and gateway providers serve as a critical choke-point for reducing the number of illegal robocalls received by American consumers. In the Gateway Provider Report and Order, the Commission took steps to prevent these foreign-originated illegal robocalls from reaching consumers and to help track these calls back to the source. Along with further extension of the Commission’s caller ID authentication requirements and Robocall Mitigation Database filing requirements, the Commission adopted several robocall mitigation requirements, including a requirement for gateway providers to respond to traceback within 24 hours, mandatory blocking requirements, a “know your upstream provider” requirement, and a general mitigation requirement. |
- | 3060-1303 | ||
| 202511-0607-002 | Monthly Retail Surveys | DOC/CENSUS | 2025-12-04 | None | None | Received in OIRA | Extension without change of a currently approved collection
Monthly Retail Surveys
Key Information
Abstract
The Monthly Retail Surveys (MRS), comprised of the Monthly Retail Trade Survey (MRTS) and the Advanced Monthly Retail Survey (MARTS), provide estimates of monthly retail sales, end-of-month merchandise inventories, and quarterly e-commerce sales of retailers in the United States by selected kinds of business. They also provide monthly sales of food service establishments. The Bureau of Economic Analysis (BEA) uses this information to prepare the National Income and Products Accounts and to benchmark the annual input-output tables. Statistics provided are used to calculate the gross domestic product (GDP). |
- | 0607-0717 | ||
| 202504-0910-001 | Authorization of Medical Products for Use Emergencies | HHS/FDA | 2025-12-04 | None | None | Received in OIRA | Reinstatement without change of a previously approved collection
Authorization of Medical Products for Use Emergencies
Key Information
Abstract
This Information Collection Request (ICR) collects information from manufacturers and public health authorities applicable to the authorization of the emergency use of certain medical products during a declared emergency. Respondents submit information as recommended in Food and Drug Administration (FDA or Agency) guidance, including a description of the medical product and the intended use, reports after administration of such a product, and requests for extension of the expiration date of eligible products. |
- | 0910-0595 | ||
| 202509-2577-004 | Public Housing Authority Executive Compensation Information | HUD/PIH | 2025-12-04 | None | None | Received in OIRA | Reinstatement with change of a previously approved collection
Public Housing Authority Executive Compensation Information
Key Information
Abstract
HUD will collect and make transparent information on the top management official, top financial official, and highest compensated employee at public housing agencies (PHAs.) |
- | 2577-0272 | ||
| 202509-3235-010 | Rule 17a-4; Records to be Preserved by Certain Exchange Members, Brokers and Dealers | SEC | 2025-12-04 | None | None | Received in OIRA | Extension without change of a currently approved collection
Rule 17a-4; Records to be Preserved by Certain Exchange Members, Brokers and Dealers
Key Information
Abstract
Rule 17a-4, 17 CFR 240.17a-4, requires certain records to be maintained by certain exchange members, registered brokers and dealers, and other respondents. The collection of information helps ensure that respondents are in compliance with certain laws, rules, and regulations. |
- | 3235-0279 | ||
| 202507-3038-002 | Rule 50.50 End-User Notification of Non-Cleared Swap | CFTC | 2025-12-04 | None | None | Received in OIRA | Extension without change of a currently approved collection
Rule 50.50 End-User Notification of Non-Cleared Swap
Key Information
Abstract
Section 2(h)(1)(A) of the Commodity Exchange Act requires certain entities to submit for clearing certain swaps if they are required to be cleared by the Commission. Section 2(h)(7)(a) provides that non-financial end-users using swaps to hedge or mitigate commercial risk may elect not to clear swaps that otherwise would be required to be cleared, if they satisfy certain conditions. Similarly, Rule 50.50 permits certain end-user entities to elect not to clear swaps that otherwise would be required to be cleared, provided that they satisfy certain conditions. The rule further requires the reporting of certain information if the exception is elected. This collection pertains to information the Commission needs to monitor use of the end-user exception, to prevent abuse of the end-user election, and to assess market risk in connection therewith. |
- | 3038-0085 | ||
| 202512-0938-007 | Accreditation of Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS) Suppliers (CMS-10932) | HHS/CMS | 2025-12-03 | None | None | Received in OIRA | New collection (Request for a new OMB Control Number)
Accreditation of Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS) Suppliers (CMS-10932)
Key Information
Authorizing Statutes
Abstract
Since 2006, DMEPOS suppliers have been required to be accredited by a CMS-approved DMEPOS accreditation organization (AO) in order to enroll in Medicare. The accreditation process, which typically centers around the AO’s on-site survey of the DMEPOS supplier, is designed to help confirm that the supplier is compliant with the DMEPOS quality standards. To become and remain a DMEPOS AO – of which there currently are eight -- an organization must comply with the requirements of § 424.58. These requirements include, but are not limited to, submission of: (i) an initial application to CMS to become a DMEPOS AO; (ii) an application to CMS for reapproval as a DMEPOS AO; and (iii) periodic information to CMS about its DMEPOS accreditation program. These AO applications and data submissions do not follow a specific format and are not furnished on uniform OMB-approved forms -- akin to, for example, the Form CMS-855S DMEPOS supplier enrollment application (Medicare Enrollment Application - Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS) Suppliers; OMB Control Number: 0938-1056). CMS on July 2, 2025, published in the Federal Register a proposed rule titled, “Medicare and Medicaid Programs; Calendar Year 2026 Home Health Prospective Payment System (HH PPS) Rate Update; Requirements for the HH Quality Reporting Program and the HH Value-Based Purchasing Expanded Model; Durable Medical Equipment, Prosthetics, Orthotics, and Supplies (DMEPOS) Competitive Bidding Program Updates; DMEPOS Accreditation Requirements; and Other Medicare and Medicaid Policies” (90 FR 29108) (CMS-1828-P). Among the proposals in this proposed rule were additional requirements that organizations must meet to become or remain a DMEPOS AO. These proposals would: (1) facilitate greater CMS oversight of the DMEPOS accreditation program in general and DMEPOS AOs in particular; and (2) help better ensure that DMEPOS AOs are adequately performing their accreditation and quality standard verification activities. These requirements would be included in revised § 424.58. |
- | 0938-1484 | ||
| 202508-3235-006 | Form S-3 - Registration Statement | SEC | 2025-12-03 | None | None | Received in OIRA | Extension without change of a currently approved collection
Form S-3 - Registration Statement
Key Information
Authorizing Statutes
Abstract
The Securities Act of 1933 (“Securities Act”) was designed to prevent misrepresentation, deceit and other fraudulent acts and practices in the sale of securities. Section 5 of the Securities Act requires that a registration statement be filed before any security is publicly offered, and that the registration statement be effective before any security is sold. Section 7 of the Securities Act and Schedule A outlines the information that must be contained in a registration statement. Section 7 gives the Commission the authority to vary such disclosure for various classes of issuers and securities. The Commission has used its statutory authority to develop a number of specialized registration statement forms that tailor disclosure requirements based on the type of offering, issuer, or other parameters, thereby eliminating burdensome and unnecessary requirements while maintaining investor protection. Form S-3 (17 CFR 239.13) is a short-form securities registration statement that is available to issuers that meet certain registrant and transaction eligibility requirements under the form. The purpose of the information collection is to provide disclosure of material financial and other information with which investors may evaluate the merits of securities in order to make investment decisions. |
- | 3235-0073 | ||
| 202507-1010-002 | Renewable Energy and Alternate Uses of Existing Facilities on the Outer Continental Shelf (30 CFR 585 and 586) | DOI/BOEM | 2025-12-03 | None | None | Received in OIRA | Revision of a currently approved collection
Renewable Energy and Alternate Uses of Existing Facilities on the Outer Continental Shelf (30 CFR 585 and 586)
Key Information
Abstract
This information collection request addresses the paperwork requirements in the regulations under 30 CFR parts 585 and 586 issued pursuant to the OCS Lands Act, as amended (43 U.S.C. 1331 et seq.). The OCS Lands Act at subsection 8(p) (43 U.S.C. 1337(p)) authorizes the Secretary of the Interior to issue leases, easements, or rights-of-way on the OCS for activities that produce or support production, transportation, or transmission of energy from sources other than oil and gas, including renewable energy. Subsection 8(p) directs the Secretary to issue any necessary regulations to carry out the OCS renewable energy program. The Secretary delegated this authority to BOEM. BOEM issued regulations for OCS renewable energy activities at 30 CFR parts 585 and 586; this notice concerns the reporting and recordkeeping elements required by these regulations. |
- | 1010-0176 | ||
| 202510-0648-001 | Alaska Chinook Salmon Economic Data Report (EDR) | DOC/NOAA | 2025-12-03 | None | None | Received in OIRA | Extension without change of a currently approved collection
Alaska Chinook Salmon Economic Data Report (EDR)
Key Information
Abstract
This is a request by the National Marine Fisheries Service (NMFS) Alaska Region for extension of this currently approved information collection for the Annual Alaska Chinook Salmon Economic Data Report (Chinook Salmon EDR). The Chinook Salmon EDR evaluates the effectiveness of Chinook salmon bycatch management measures for the Bering Sea pollock fishery that were implemented under Amendment 91 to the Fishery Management Plan (FMP) for Groundfish of the Bering Sea and Aleutian Islands (BSAI) Management Area. The Chinook Salmon EDR Program provides information to the NMFS analysts and North Pacific Fisheries Management Council staff. It is intended to be used to evaluate the effectiveness of the Chinook Salmon Incentive Plan Agreement (IPA) (see OMB Control No. 0648-0401); to evaluate where, when, and how pollock fishing and salmon bycatch occur; and to provide data to study and verify conclusions drawn by industry in the IPA annual reports. |
- | 0648-0633 | ||
| 202508-3235-003 | Form S-1 Registration Statement | SEC | 2025-12-03 | None | None | Received in OIRA | Extension without change of a currently approved collection
Form S-1 Registration Statement
Key Information
Authorizing Statutes
Abstract
The Securities Act of 1933 (the “Securities Act”) was enacted in order to provide full and fair disclosure with respect to publicly offered securities and to prevent fraud in connection with such offerings. The Securities Act carries out this purpose by requiring the filing of a registration statement in connection with public distributions of securities by issuers and their control persons. Schedule A of the Securities Act specifies the general types of information that must be disclosed in registration statements filed with the Securities and Exchange Commission (“Commission”). The Commission has authority, under Section 19 of the Securities Act, to promulgate rules to carry out the provisions of the Securities Act. Form S-1 (17 CFR 239.11) is a general registration form used to register the public offering of securities under the Securities Act of 1933 (“Securities Act”). Form S-1 may be used for the registration under the Securities Act of securities of all registrants for which no other form is authorized or prescribed, except that this Form shall not be used for securities of foreign governments or political subdivisions thereof or asset-backed securities. The information collected is intended to ensure the adequacy of information available to investors in connection with securities offerings. |
- | 3235-0065 | ||
| 202509-3235-009 | Rule 30e-3 (17 CFR 270.30e-3) under the Investment Company Act of 1940, "Internet availability of reports to shareholders" | SEC | 2025-12-03 | None | None | Received in OIRA | Extension without change of a currently approved collection
Rule 30e-3 (17 CFR 270.30e-3) under the Investment Company Act of 1940, "Internet availability of reports to shareholders"
Key Information
Abstract
Rule 30e-3 (17 CFR 270.30e-3) under the Investment Company Act of 1940, as amended, provides an optional method for a management company registered on Form N-2 or Form N-3 and any separate series of the management company that is required to transmit a report to shareholders pursuant to rule 30e-1 (17 CFR 270.30e-1) under the Investment Company Act of 1940, as amended, to satisfy shareholder report transmission requirements by making such reports and certain other materials publicly accessible on a website, as long as they satisfy certain other conditions of the rule. Reliance on the rule is voluntary to satisfy the reporting requirement. |
- | 3235-0758 | ||
| 202511-3060-023 | Local Telephone Competition and Broadband Reporting, Report and Order, FCC Form 477 (WC Docket No. 19-195, WC Docket No. 11-10, FCC 19-79) | FCC | 2025-12-03 | None | None | Received in OIRA | Extension without change of a currently approved collection
Local Telephone Competition and Broadband Reporting, Report and Order, FCC Form 477 (WC Docket No. 19-195, WC Docket No. 11-10, FCC 19-79)
Key Information
Authorizing Statutes
Abstract
This collection involves information about broadband connections to end-user locations, wired and wireless local telephone services, and interconnected Voice over Internet Protocol (VOIP) services in the 50 states, the District of Columbia, and the Territories and possessions. Data obtained from this collection will be used to prepare reports that will help consumers, policy makers, government agencies, analysts, and others to determine broadband service availability by provider, technology, and speed. |
- | 3060-0816 | ||
| 202511-0910-004 | Small Dispensers Assessment Under the Drug Supply Chain Security Act | HHS/FDA | 2025-12-03 | None | None | Received in OIRA | New collection (Request for a new OMB Control Number)
Small Dispensers Assessment Under the Drug Supply Chain Security Act
Key InformationAbstract
The purpose of this statutorily required study is to assess the feasibility of dispensers with 25 or fewer full-time employees conducting interoperable, electronic tracing of products at the package level. Research questions include the accessibility of the necessary software and hardware to such dispensers; whether the necessary software and hardware is prohibitively expensive to obtain, install, and maintain for such dispensers; and if the necessary hardware and software can be integrated into business practices. Small dispensers of prescription drug products will be recruited to access and respond to the assessment questions on FDA's web site. Evaluation methods and analyses include qualitative analyses (for example, content analysis for responses), and quantitative analyses using descriptive statistics. |
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| 202512-3048-004 | EIB 15-04 Exporter’s Certificate For Co-Financed Loan, Guarantee & MT Insurance Programs | EXIMBANK | 2025-12-02 | None | None | Received in OIRA | Revision of a currently approved collection
EIB 15-04 Exporter’s Certificate For Co-Financed Loan, Guarantee & MT Insurance Programs
Key Information
Abstract
EXIM Bank’s borrowers, financial institution policy holders and guaranteed lenders provide this form to U.S. exporters, who certify to the eligibility of their exports for EXIM Bank support. For loan guarantees, the completed form is required to be submitted at time of disbursement and held by either the guaranteed lender or EXIM Bank. For MT insurance, the completed forms are held by the financial institution, only to be submitted to EXIM Bank in the event of a claim filing. EXIM Bank uses the referenced form to obtain exporter certifications regarding the export transaction, content sourcing, and their eligibility to participate in USG programs with respect to co-financed transactions. These details are necessary to determine the value and legitimacy of EXIM Bank financing support and claims submitted. It also provides the financial institutions a check on the export transaction’s eligibility at the time it is fulfilling a financing request. |
- | 3048-0052 | ||
| 202512-0938-002 | CLIA Proficiency Testing (PT) (CMS-10690) | HHS/CMS | 2025-12-02 | None | None | Received in OIRA | 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. |
- | 0938-1357 | ||
| 202512-3048-003 | MT MGA Disbursement Approval Request | EXIMBANK | 2025-12-02 | None | None | Received in OIRA | Extension without change of a currently approved collection
MT MGA Disbursement Approval Request
Key Information
Abstract
The Export Import Bank of the United States (EXIM 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, EXIM 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 EXIM Bank assistance. This form will enable EXIM Bank to identify the specific details of the export transaction. These details are necessary for determining the eligibility of disbursements for approval. |
- | 3048-0049 | ||
| 202512-3048-002 | Credit Guarantee Facility Disbursement Approval Request | EXIMBANK | 2025-12-02 | None | None | Received in OIRA | 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. |
- | 3048-0046 | ||
| 202512-3048-001 | Payment Default Report | EXIMBANK | 2025-12-02 | None | None | Received in OIRA | 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. |
- | 3048-0028 | ||
| 202512-0938-004 | CAHPS Home Health Care Survey (CMS-10275) | HHS/CMS | 2025-12-02 | None | None | Received in OIRA | 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. |
- | 0938-1066 | ||
| 202512-0920-001 | [NCHS] Division of Vital Statistics Proposal for Access to Restricted-Use Data for the National Center for Health Statistics | HHS/CDC | 2025-12-01 | None | None | Received in OIRA | 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 InformationAbstract
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. |
- | |||
| 202511-1910-001 | Events, Meetings, and Registrations | DOE/DOEOA | 2025-12-01 | None | None | Received in OIRA | New collection (Request for a new OMB Control Number)
Events, Meetings, and Registrations
Key InformationAbstract
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. |
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| 202507-2120-006 | Suspected Unapproved Parts Notification | DOT/FAA | 2025-12-01 | None | None | Received in OIRA | 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. |
- | 2120-0552 | ||
| 202511-1670-001 | SAFECOM Nationwide Surveys Generic Clearance | DHS/CISA | 2025-12-01 | None | None | Received in OIRA | Extension without change of a currently approved collection
SAFECOM Nationwide Surveys Generic Clearance
Key Information
Authorizing Statutes
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). |
- | 1670-0048 |