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 15149 results

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

Title:

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

Reference Number:

202410-0910-006

Omb Control Number:

0910-0775

Agency:

HHS/FDA

Received:

2024-10-25

Concluded:

2025-01-03

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
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

Presidential Action:

-

Title:

Guidance on Meetings with Industry and Investigators on the Research and Development of Tobacco Products

Reference Number:

202410-0910-008

Omb Control Number:

0910-0731

Agency:

HHS/FDA

Received:

2024-10-25

Concluded:

2025-01-03

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Guidance on Meetings with Industry and Investigators on the Research and Development of Tobacco Products

Key Information

Abstract

This ICR is for a guidance intended to assist tobacco manufacturers, importers, researchers, and investigators, and their representatives who seek meetings with staff of FDA’s Center for Tobacco Products (CTP). This guidance does not pertain to other types of meetings or meeting requests with CTP staff. The Federal Food, Drug, and Cosmetic Act (FD&C Act), as amended by the Family Smoking Prevention and Tobacco Control Act (Tobacco Control Act) offers several pathways to obtain an order from FDA to authorize the marketing of a new tobacco product before it may be introduced or delivered into interstate commerce. To provide assistance with these pathways to market products, FDA will meet with tobacco product manufacturers, importers, researchers, and investigators (or their representatives) where appropriate. This guidance is intended to assist persons who seek guidance relating to their research to inform the regulation of tobacco products or to support the development or marketing of tobacco products. This guidance describes two collections of information: (1) The submission of a meeting request containing certain information and (2) the submission of a meeting information package in advance of the meeting. The purpose of the meeting information package is to provide Agency staff the opportunity to adequately prepare for the meeting, including the review of relevant data concerning the product. In the Agency’s experience, reviewing such information is critical to achieving a productive meeting. For information that was previously submitted in a meeting request, the information package should provide updated information that reflects the most current and accurate information available.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 111 - 111 31
View Law

Presidential Action:

-

Title:

Tobacco Health Document Submission

Reference Number:

202410-0910-011

Omb Control Number:

0910-0654

Agency:

HHS/FDA

Received:

2024-10-25

Concluded:

2025-01-03

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Tobacco Health Document Submission

Key Information

Abstract

In the guidance document, FDA requests tobacco health document submissions from manufacturers and importers of tobacco products based on the statutory requirements and compliance dates. As indicated in the guidance, all manufacturers and importers of tobacco products are required to provide immediate and ongoing submission of health documents developed after June 22, 2009. However, FDA generally does not intend to enforce the requirement at this time with respect to all such health documents, so long as a specified set of documents, those developed between June 23, 2009, and December 31, 2009, are provided at least 90 days prior to the delivery for introduction of tobacco products into interstate commerce. Thereafter, manufacturers should preserve all health documents, including those that relate to products for further manufacturing and those developed after December 31, 2009, for future submission to FDA. Respondents submit information through a facilitative electronic form or in paper form using Form FDA 3743. In both forms, FDA requests information including: submitter identification, submitter point of contact, submission format and contents (as applicable), confirmation statement, document categorization (as applicable), document readability and accessibility, and document metadata. The information collected will inform FDA's regulatory processes and decision making such as, development of good manufacturing practices, review standards for new tobacco products, and regulation of modified risk tobacco products, among others.

Federal Register Notices

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

Authorizing Statutes

21 USC 904(a)(4)
View Law

Presidential Action:

-

Title:

Tobacco Products, Exemptions From Substantial Equivalence Requirements

Reference Number:

202410-0910-009

Omb Control Number:

0910-0684

Agency:

HHS/FDA

Received:

2024-10-25

Concluded:

2025-01-03

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Tobacco Products, Exemptions From Substantial Equivalence Requirements

Key Information

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

21 USC 387e
View Law
Pub.L. 111 - 111 31
View Law

Presidential Action:

-

Title:

Regulation of Domestic Exchange-Traded Options

Reference Number:

202407-3038-004

Omb Control Number:

3038-0007

Agency:

CFTC

Received:

2024-10-25

Concluded:

2024-12-30

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Regulation of Domestic Exchange-Traded Options

Key Information

Abstract

The Commodity Futures Trading Commission (“Commission”) has promulgated Commission Regulations 33.7 and 33.8, respectively, which require futures commission merchants (“FCMs”) and introducing brokers (“IBs”): (1) to provide retail (i.e., non-eligible contract participant) customers with, and retain, standard risk disclosure statements concerning the risk of trading certain domestic exchange-traded commodity options; and (2) to retain all related promotional material and the source of authority for information contained therein. These requirements help assure that these customers are not fraudulently induced to invest in these commodity options by persons who misrepresent the risks of such transactions. The recordkeeping requirements assist the Commission and the National Futures Association (“NFA”) in verifying registrants’ compliance with their disclosure obligations and ensuring that related promotional material is not fraudulent or misleading.

Federal Register Notices

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

Authorizing Statutes

7 USC 1a
View Law
7 USC 4
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7 USC 6, 6a, 6b, 6c, 6d, 6e, 6f, 6g
View Law
7 USC 6h, 6i, 6j, 6k, 6l, 6m, 6n, 6o
View Law
7 USC 7, 7a, 7b
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7 USC 8
View Law
7 USC 9
View Law
7 USC 11
View Law
7 USC 12a, 12c
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7 USC 13a, 13a-1, 13b
View Law
7 USC 19
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7 USC 21
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7 USC 2
View Law

Presidential Action:

-

Title:

Regulations Restricting the Sale and Distribution of Cigarettes and Smokeless Tobacco to Protect Children and Adolescents

Reference Number:

202410-0910-012

Omb Control Number:

0910-0312

Agency:

HHS/FDA

Received:

2024-10-25

Concluded:

2025-01-03

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Regulations Restricting the Sale and Distribution of Cigarettes and Smokeless Tobacco to Protect Children and Adolescents

Key Information

Abstract

This collection includes reporting information requirements for § 1140.30 and associated guidance, which direct persons to notify FDA if they intend to use a form of advertising that is not addressed in the regulations.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 111 - 31 102
View Law

Presidential Action:

-

Title:

Market Data Infrastructure -- Rule 614(d)(9)

Reference Number:

202410-3235-011

Omb Control Number:

3235-0794

Agency:

SEC

Received:

2024-10-25

Concluded:

2024-12-09

Action:

Approved without change

Status:

Active

Request Type:

New collection (Request for a new OMB Control Number)
Market Data Infrastructure -- Rule 614(d)(9)

Key Information

Abstract

The Commission adopted Rule 614(d)(9) for competing consolidators that do not meet a revenue threshold that will imposes obligations which are substantially similar to certain Regulation SCI requirements.

Federal Register Notices

60-Day FRN
View Notice

Authorizing Statutes

17 USC 78a et seq
View Law

Presidential Action:

-

Title:

Evaluation of Public Visitors' Experience at the National Marine Sanctuaries Visitor Centers and Exhibits

Reference Number:

202410-0648-005

Omb Control Number:

0648-0582

Agency:

DOC/NOAA

Received:

2024-10-25

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
Evaluation of Public Visitors' Experience at the National Marine Sanctuaries Visitor Centers and Exhibits

Key Information

Abstract

This request is for the extension of a current information collection. The evaluation of visitor demographics, experiences, and opinions about visitor centers and exhibits is needed to support the conservation, education, and management goals of the National Oceanic and Atmospheric Administration Office of National Marine Sanctuaries (ONMS) to strengthen and improve the stewardship, sustainable use, and protection of natural, cultural, and historical resources. Under the jurisdiction of ONMS and to satisfy legal mandates, the National Oceanic and Atmospheric Administration (NOAA) is authorized to conduct evaluations, such as this information collection, under the American Innovation and Competitiveness Act (Section 314(c), codified at 33 U.S.C. § 893(a)) to ensure education programs have measurable objectives and milestones, as well as clear, documented metrics for evaluating its programs. We therefore are seeking to find out if people visiting ONMS’ visitor centers and exhibits are receiving our new messages by conducting an optional exit survey. Conducting thorough evaluations will aid in vital decisions regarding exhibit renovation, new exhibits, interpretation programs, and educational content.

Federal Register Notices

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

Authorizing Statutes

16 USC 1431 et seq.
View Law
Pub.L. 114 - 329 314(c)
View Law

Presidential Action:

-

Title:

Pre-Employment Drug Policy Notification and Acknowledgement (DEA-200)

Reference Number:

202407-1117-001

Omb Control Number:

1117-0063

Agency:

DOJ/DEA

Received:

2024-10-25

Concluded:

2024-10-28

Action:

Approved without change

Status:

Active

Request Type:

New collection (Request for a new OMB Control Number)
Pre-Employment Drug Policy Notification and Acknowledgement (DEA-200)

Key Information

Abstract

Applicants for employment with the Drug Enforcement Administration must complete this form and submit it as part of their employment application. This form requests information related to an applicant's drug usage.

Federal Register Notices

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

Presidential Action:

-

Title:

Warning Plans for Smokeless Tobacco Products

Reference Number:

202410-0910-010

Omb Control Number:

0910-0671

Agency:

HHS/FDA

Received:

2024-10-25

Concluded:

2025-01-03

Action:

Approved without change

Status:

Active

Request Type:

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.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 113 - 31 3
View Law
15 USC 4402
View Law

Presidential Action:

-

Title:

Reporting Harmful and Potentially Harmful Constituents in Tobacco Products and Tobacco Smoke Under the Federal Food, Drug, and Cosmetic Act

Reference Number:

202410-0910-007

Omb Control Number:

0910-0732

Agency:

HHS/FDA

Received:

2024-10-25

Concluded:

2025-01-03

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Reporting Harmful and Potentially Harmful Constituents in Tobacco Products and Tobacco Smoke Under the Federal Food, Drug, and Cosmetic Act

Key Information

Abstract

This collection requires each tobacco product manufacturer or importer, or an agent, to report to FDA "all constituents, including smoke constituents, identified by [FDA] as harmful or potentially harmful to health in each tobacco product, and as applicable in the smoke of each tobacco product." These entities must also provide similar information at least 90 days prior to introducing the product into interstate commerce.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 111 - 111 31
View Law

Presidential Action:

-

Title:

Various International Agreement Safety Certificates and Documents

Reference Number:

202407-1625-005

Omb Control Number:

1625-0017

Agency:

DHS/USCG

Received:

2024-10-24

Concluded:

2025-02-27

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Various International Agreement Safety Certificates and Documents

Key Information

Abstract

These Coast Guard-issued forms are used as evidence of compliance with the International Convention for Safety of Life at Sea, 1974 by certain U.S. vessels on international voyages. Without the proper certificates or documents, a U.S. vessel could be detained in foreign ports. The statutory authority is 46 U.S. Code 3306, 3307, 3316 and 3703.

Federal Register Notices

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

Authorizing Statutes

46 USC 3316
View Law
46 USC 3307
View Law
46 USC 3703
View Law
46 USC 3306
View Law

Presidential Action:

-

Title:

Exchange Act Form 10-D

Reference Number:

202408-3235-015

Omb Control Number:

3235-0604

Agency:

SEC

Received:

2024-10-24

Concluded:

2024-12-30

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Exchange Act Form 10-D

Key Information

Abstract

Form 10-D is used for distribution reports filed by asset-backed securities issuers pursuant to Sections 13 and 15(d) of the Exchange Act of 1934.

Federal Register Notices

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

Authorizing Statutes

15 USC 78m, 78o(d), 78w(a), 78ll
View Law

Presidential Action:

-

Title:

Standards of Training, Certification and Watchkeeping for Seafarers (STCW), International Convention

Reference Number:

202406-1625-009

Omb Control Number:

1625-0079

Agency:

DHS/USCG

Received:

2024-10-24

Concluded:

2025-06-18

Action:

Comment filed on proposed rule and continue

Status:

Historical Inactive

Request Type:

Revision of a currently approved collection
Standards of Training, Certification and Watchkeeping for Seafarers (STCW), International Convention

Key Information

Abstract

This information is necessary to ensure compliance with the international requirements of the STCW Convention, and to maintain an acceptable level of quality in activities associated with training and assessment of merchant mariners. Respondents are owners and operators of vessels, training institutions, and mariners. 46 U.S. Code (U.S.C.) Chapter 71 is the statutory authority.

Federal Register Notices

60-Day FRN
View Notice

Authorizing Statutes

46 USC 71
View Law

Presidential Action:

-

Title:

Report of Marine Casualty & Chemical Testing of Commercial Vessel Personnel

Reference Number:

202306-1625-002

Omb Control Number:

1625-0001

Agency:

DHS/USCG

Received:

2024-10-24

Concluded:

2025-06-18

Action:

Comment filed on proposed rule and continue

Status:

Historical Inactive

Request Type:

Revision of a currently approved collection
Report of Marine Casualty & Chemical Testing of Commercial Vessel Personnel

Key Information

Abstract

Marine casualty information is needed for CG investigations of commercial vessel casualties involving death, vessel damage, etc., as mandated by Congress. Chemical testing information is needed to improve CG detection/reduction of drug and alcohol use by mariners. The statutory authority for the requirements is 18 U.S.C. Chapter 17A, 43 U.S.C. 1333, 46 U.S.C. 2103, 2302, 2303a, 2306, 3306, 6101, 6301, 6305, 7101, 7301, 7503, 7701, 7704, 56311 and 70034.

Federal Register Notices

60-Day FRN
View Notice

Authorizing Statutes

46 USC 7301
View Law
46 USC 7701
View Law
46 USC 56311
View Law
46 USC 7704
View Law
46 USC 6101
View Law
18 USC Chapter 17A
View Law
46 USC 6301
View Law
46 USC 2302
View Law
46 USC 70034
View Law
46 USC 2103
View Law
46 USC 7503
View Law
46 USC 2303A
View Law
46 USC 2306
View Law
46 USC 3306
View Law
46 USC 6305
View Law
46 USC 7101
View Law

Presidential Action:

-

Title:

10 CFR Part 50, Domestic Licensing of Production and Utilization Facilities

Reference Number:

202410-3150-005

Omb Control Number:

3150-0011

Agency:

NRC

Received:

2024-10-24

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
10 CFR Part 50, Domestic Licensing of Production and Utilization Facilities

Key Information

Abstract

Part 50 of title 10 of the Code of Federal Regulations (10 CFR), “Domestic Licensing of Production and Utilization Facilities,” specifies technical information and data to be provided to the NRC or maintained by applicants and licensees so that the NRC may take determinations necessary to protect the health and safety of the public, in accordance with the Atomic Energy Act of 1954, as amended. The reporting and recordkeeping requirements contained in 10 CFR part 50 are mandatory for the affected licensees and applicants.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 83 - 703 68 Stat. 919
View Law
Pub.L. 109 - 58 119 Stat 594
View Law

Presidential Action:

-

Title:

[Medicaid] Medicaid Managed Care and Supporting Regulations (CMS-10855)

Reference Number:

202408-0938-004

Omb Control Number:

0938-1445

Agency:

HHS/CMS

Received:

2024-10-24

Concluded:

2025-01-17

Action:

Approved without change

Status:

Active

Request Type:

New collection (Request for a new OMB Control Number)
[Medicaid] Medicaid Managed Care and Supporting Regulations (CMS-10855)

Key Information

Abstract

This collection of information request is associated with our September 26, 2024 (89 FR 79020) final rule (CMS-2434-F; RIN 0938-AU28). We intend to fold the following collection of information requirements and burden estimates under CMS-10108 (OMB 0938-0920). However, there are a number of conflicting activities that make this impractical at this time. To address those conflicts, as a stop gap measure we are proposing to submit the collection of information requirements and burden estimates under CMS-10855 (OMB 0938-1445). When ready we will be folding them to their proper place under CMS-10108 (OMB 0938-0920). Most Medicaid beneficiaries receive either all or part of their health care benefits through Medicaid managed care programs, including their prescription drug benefits. Because of the specialized nature of the prescription drug benefit, many of the Medicaid managed care plans (MCOs, PIHPS, or PAHPS) either own, or contract with, PBMs to administer the pharmacy benefit. In § 438.3(s), Medicaid MCOs, PIHPs, and PAHPs that provide coverage of covered outpatient drugs (CODs) would be required to structure any contract that it has with any subcontractor (e.g., PBM) for the delivery or administration of the COD benefit so that the subcontractor is required to report separately the amounts related to the incurred claims described in § 438.8(e)(2) to the managed care plan. The provisions would ensure that medical loss ratios (MLRs) reported by MCOs, PIHPs and PAHPs that use subcontractors in the delivery of COD coverage would be more accurate and transparent. The separate payment requirements would help States and managed care plans better understand whether they are appropriately and efficiently paying for the delivery of CODs, a significant part of which is funded by the Federal Government.

Federal Register Notices

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

Authorizing Statutes

42 USC 1396a
View Law

Presidential Action:

-

Title:

Child and Adult Care Food Program (CACFP)

Reference Number:

202410-0584-005

Omb Control Number:

0584-0055

Agency:

USDA/FNS

Received:

2024-10-24

Concluded:

2024-10-29

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Child and Adult Care Food Program (CACFP)

Key Information

Abstract

This is a non-substantive change request to upload the correct burden chart, burden narrative, and regulation attachments for the submission related to the final rule, Child Nutrition Programs: Meal Patterns Consistent with the 2020-2025 Dietary Guidelines for Americans. The attachments from another collection impacted by this rule, OMB Control Number 0584-0280 7 CFR Part 225 Summer Food Service Program, were accidentally uploaded into this entry. This request does not impact the burden estimates or other data provided for the final rule submission. The Child and Adult Care Food Program (CACFP) provides cash reimbursement and commodity assistance, on a per meal basis, for food service to children in nonresidential childcare centers and family day care homes, and to eligible adults in nonresidential adult day care centers. The USDA, through FNS, has established application, monitoring, and reporting requirements to manage the CACFP effectively.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 111 - 296 10
View Law
42 USC 1751 et. seq
View Law

Presidential Action:

-

Title:

Prohibition of Payment of SSI Benefits to Fugitive Felons and Parole/Probation Violators

Reference Number:

202410-0960-005

Omb Control Number:

0960-0617

Agency:

SSA

Received:

2024-10-24

Concluded:

2025-02-26

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Prohibition of Payment of SSI Benefits to Fugitive Felons and Parole/Probation Violators

Key Information

Abstract

Section 1611(e)(4) of the Act precludes eligibility for SSI payments for certain fugitives and probation or parole violators. Our regulation at 20 CFR 416.708(o) requires individuals applying for or receiving SSI to report to SSA that: (1) they are fleeing to avoid prosecution for a crime; (2) they are fleeing to avoid custody or confinement after conviction of a crime; or (3) they are violating a condition of probation or parole. In addition, due to the implementation of the Martinez v. Astrue and Clark v. Astrue cases, we changed our policy to deny eligibility or suspend payments for three fleeing codes. We use the information we receive to determine eligibility on an initial claim for SSI payments or a redetermination of existing recipients. The collection is mandatory to ensure that an applicant or recipient does not have a warrant for one of the three fleeing codes. If the respondent has a warrant for one of the three fleeing codes, SSA uses this information to deny payments. The respondents are SSI applicants and recipients, or their representative payees, who are reporting their status as a fugitive felon or probation or parole violator.

Federal Register Notices

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

Authorizing Statutes

42 USC 1382
View Law
42 USC 402
View Law
Pub.L. 104 - 193 Public Law 104-193
View Law

Presidential Action:

-

Title:

Media Bureau Incentive Auction Implementation, Sections 73.3700(c), (h)(5)-(6), (g)(4)

Reference Number:

202410-3060-011

Omb Control Number:

3060-1216

Agency:

FCC

Received:

2024-10-24

Concluded:

2025-01-10

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Media Bureau Incentive Auction Implementation, Sections 73.3700(c), (h)(5)-(6), (g)(4)

Key Information

Abstract

On September 19, 2023, the Commission released a Report and Order wherein it adopted several revisions to its Part 73 rules including 73.3700. As a result of these rule revisions, a number of collections and burdens were eliminated altogether. Sections 73.3700(b)(4)(i) and (ii) and 73.3700(d) of the rules were eliminated and therefore the corresponding collections and burdens for these rules have been eliminated. Also, revisions were made to estimates for 73.3700(c), 73.3700(g)(4) and 73.3700 (h)(5) and (h)(6) to reflected updated data now that the incentive auction is complete and the exact universe of affected entities is known.

Federal Register Notices

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

Authorizing Statutes

47 USC 151, 154, 301, 303, 307,
View Law
47 USC 308, 309, 310, 316, 319,
View Law
47 USC 325(b),332, 336(f), 338, 339,
View Law
47 USC 340, 399b, 403, 534, 535,
View Law
47 USC 1404, 1452, 1454.
View Law

Presidential Action:

-

Title:

Plan Approval and Records for Marine Engineering Systems -- 46 CFR Subchapter F

Reference Number:

202408-1625-003

Omb Control Number:

1625-0097

Agency:

DHS/USCG

Received:

2024-10-24

Concluded:

2025-04-22

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Plan Approval and Records for Marine Engineering Systems -- 46 CFR Subchapter F

Key Information

Abstract

This collection of information requires an owner or builder of a commercial vessel to submit to the U.S. Coast Guard for review and approval, plans pertaining to marine engineering systems to ensure that the vessel will meet regulatory standards. Respondents are owners and builders of commercial vessels. The statutory authority is 43 U.S. Code (U.S.C.) 1333 and 46 U.S.C. 3306 and 3703.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

46 USC 3703
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43 USC 1333
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46 USC 3306
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Presidential Action:

-

Title:

Request for Internet Services-Authentication; 800# Automated Telephone Speech Technology-Authentication

Reference Number:

202410-0960-004

Omb Control Number:

0960-0596

Agency:

SSA

Received:

2024-10-24

Concluded:

2025-03-04

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Request for Internet Services-Authentication; 800# Automated Telephone Speech Technology-Authentication

Key Information

Abstract

RISA, one of SSA's authentication methods, allows individuals to access their personal information through our Internet and Automated Telephone Services. SSA asks individuals and third parties who seek personal information from SSA records, or who register to participate in SSA's online business services, to provide certain identifying information. As an extra measure of protection, SSA asks requestors who use the Internet and telephone services to provide additional identifying information unique to those services so SSA can authenticate their identities before releasing personal information. The respondents are current beneficiaries who are requesting personal information from SSA, and individuals and third parties who are registering for SSA's online business services. This is a Non-Substantive Change Request to remove the burden data for the Retirement Estimator from this ICR (see Justification for details).

Federal Register Notices

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

Authorizing Statutes

42 USC 405
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Presidential Action:

-

Title:

Energy and Jobs Survey

Reference Number:

202410-1910-001

Omb Control Number:

1910-5179

Agency:

DOE/DOEOA

Received:

2024-10-24

Concluded:

2024-12-06

Action:

Approved with change

Status:

Active

Request Type:

Revision of a currently approved collection
Energy and Jobs Survey

Key Information

Abstract

The proposed data collection will explore employment related to energy, including electric power generation, electric power transmission, distribution, and storage; energy efficiency, including heating, cooling and building envelope; fuels; and motor vehicles production. The purpose is to quantify that employment, and its distribution among different sources of energy and the technologies. This effort will collect data necessary to extrapolate this information by primary value chain activity. It will also collect information on demographics and hiring security.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Presidential Action:

-

Title:

Disability Qualification Determination

Reference Number:

202410-3037-002

Omb Control Number:

3037-0012

Agency:

CPBSD

Received:

2024-10-24

Concluded:

2025-03-17

Action:

Approved with change

Status:

Active

Request Type:

Reinstatement with change of a previously approved collection
Disability Qualification Determination

Key Information

Abstract

The form will be used by the AbilityOne Program to determine eligibility as a qualified direct labor employee whose work will be counted as hours performed by a blind or significantly disabled individual as required by the JWOD Act (41 USC 85) U.S. AbilityOne Commission Compliance Policy 51.403.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

41 USC 85
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Presidential Action:

-

Title:

Request for Certificate of Degree of Indian or Alaska Native Blood (CDIB)

Reference Number:

202405-1076-010

Omb Control Number:

1076-0153

Agency:

DOI/BIA

Received:

2024-10-24

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
Request for Certificate of Degree of Indian or Alaska Native Blood (CDIB)

Key Information

Abstract

As authorized by law, BIA provides a form which allows applicants to receive documentation of degree of Indian blood and uniform standards by which we issue, amend, or invalidate a CDIB.

Federal Register Notices

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

25 USC 46 et seq.
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25 USC 450 et seq.
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25 USC 458aa et seq.
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25 USC 2001 et seq.
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61 Stat. 731
25 USC 21
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25 USC 2007
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25 USC 2201
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43 USC 1601-1624
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25 USC 13
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Presidential Action:

-
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