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 15563 results

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

Title:

[OPHDST] National Notifiable Diseases Surveillance System (NNDSS)

Reference Number:

202504-0920-009

Omb Control Number:

0920-0728

Agency:

HHS/CDC

Received:

2025-06-26

Concluded:

2025-11-21

Action:

Approved with change

Status:

Active

Request Type:

Revision of a currently approved collection
[OPHDST] National Notifiable Diseases Surveillance System (NNDSS)

Key Information

Abstract

The National Notifiable Diseases Surveillance System (NNDSS) is the nation’s public health surveillance system used to monitor the occurrence and spread of nationally notifiable conditions. Respondents are 60 jurisdictions: public health departments in every U.S. state, New York City, Washington DC, 5 U.S. territories (American Samoa, the Commonwealth of Northern Mariana Islands, Guam, Puerto Rico, and the U.S. Virgin Islands), and 3 freely associated states (the Federated States of Micronesia, the Republic of the Marshall Islands, and the Republic of Palau). NNDSS provides the official source of statistics in the United States for nationally notifiable conditions and CDC is the sole repository for these national, population-based data. Recently the NNDSS platform was modernized and expanded as a low-cost, common portal for collecting information on other conditions. Among the thousands of diseases that affect the health of the population, CDC and the Council of State and Territorial Epidemiologists (CSTE) have prioritized the approximately 120 Nationally Notifiable Conditions as those most important for public health monitoring and response. Changes to NNDSS in this Revision include: 1) Addition of case notification data for non-pestis yersiniosis, injuries related to firearms, and Chagas disease; and 2) Processing a total of 61 new data elements for 2 conditions: Toxoplasmosis and congenital toxoplasmosis The overall burden hours decreased since the last Revision because there were less one-time burdens associated with disease-specific data elements in this Revision

SPD-15 Implementation

Yes

Federal Register Notices

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

Authorizing Statutes

42 USC 241
View Law

Presidential Action:

EO 14168 Defending Women

Title:

Interstate Shellfish Dealer's Certificate

Reference Number:

202408-0910-010

Omb Control Number:

0910-0021

Agency:

HHS/FDA

Received:

2025-06-26

Concluded:

2025-07-29

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Interstate Shellfish Dealer's Certificate

Key Information

Abstract

The information collected is used to compile, publish, and distribute a listing of approved sources of State and international certified shellfish dealers/shippers. Individual State food control officials and the food industry use the list to determine certified sources of shellfish. The information collection is also used to collect samples of shellfish along with associated sample metadata. We administer the collection in an effort to help prevent and suppress the spread of communicable diseases through shellfish, which pose a unique public health concern in that the safety of molluscan shellfish directly reflects the cleanliness of the waters where they are grown.

Federal Register Notices

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

Authorizing Statutes

42 USC 243
View Law
21 USC 372
View Law

Presidential Action:

-

Title:

Incidental Take of Marine Mammals During Specified Activities (50 CFR 18.27 and 50 CFR 18, Subpart J)

Reference Number:

202503-1018-002

Omb Control Number:

1018-0070

Agency:

DOI/FWS

Received:

2025-06-26

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Incidental Take of Marine Mammals During Specified Activities (50 CFR 18.27 and 50 CFR 18, Subpart J)

Key Information

Abstract

The Marine Mammal Protection Act (MMPA) of 1972, as amended (16 U.S.C. 1361 et seq.) imposed, with certain exceptions, a moratorium on the taking of marine mammals. Section 101(a)(5)(A) of the MMPA directs the Secretary of the Interior (Secretary) to allow, upon request by citizens of the United States, the taking of small numbers of marine mammals incidental to specified activities (other than commercial fishing) if the Secretary makes certain findings and prescribes specific regulations that, among other things, establish permissible methods of taking. Once the U.S. Fish and Wildlife Service (Service or we) issue specific regulations, applicants seeking to conduct activities must request a Letter of Authorization (LOA) for the specific activity and submit onsite monitoring reports and a final report of the activity to the Secretary. Procedural regulations outlining the requirements for the submission of a request are contained in 50 CFR 18.27. We request OMB approval of the specific regulations governing authorized incidental take of marine mammals activities as separate control numbers for each subpart to facilitate simultaneous rulemaking actions when we receive applications for an ITR.

Federal Register Notices

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

Authorizing Statutes

16 USC 1361 et seq.
View Law

Presidential Action:

-

Title:

[NCEZID] DFWED National Hypothesis Generation and Investigation Module

Reference Number:

202501-0920-007

Omb Control Number:

0920-1462

Agency:

HHS/CDC

Received:

2025-06-26

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

New collection (Request for a new OMB Control Number)
[NCEZID] DFWED National Hypothesis Generation and Investigation Module

Key Information

Abstract

The goal of this package is to define a core set of data elements to be used for hypothesis generation as part of investigations of clusters or outbreaks of foodborne, waterborne, and other enteric diseases. These instruments will be used by federal, state, and local public health officials responsible for conducting interviews with reported cases in their jurisdiction in order to systematically assess core exposure elements and risk factors among cases.

SPD-15 Implementation

Yes

Federal Register Notices

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

Authorizing Statutes

42 USC 241
View Law

Presidential Action:

-

Title:

[NCBDDD] Documenting Outcomes Associated with Persistent Tic Disorders (Including Tourette Syndrome) in Children, Adolescents, and Young Adults Through Surveillance

Reference Number:

202504-0920-027

Omb Control Number:

0920-1464

Agency:

HHS/CDC

Received:

2025-06-26

Concluded:

2025-09-24

Action:

Approved with change

Status:

Active

Request Type:

New collection (Request for a new OMB Control Number)
[NCBDDD] Documenting Outcomes Associated with Persistent Tic Disorders (Including Tourette Syndrome) in Children, Adolescents, and Young Adults Through Surveillance

Key Information

Abstract

This project will collect data to describe the public health impact of persistent tic disorders including Tourette syndrome (PTD/TS) among diverse populations of children, adolescents, and young adults (i.e., aged 4 to 26 years) identified in clinical settings. Data will be collected once from a respondent (i.e., individuals with PTD/TS and their caregiver, if individual is <18 years), via a survey. These data will inform future education and outreach activities.

Federal Register Notices

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

Authorizing Statutes

42 USC 241(a) and 247b-4
View Law

Presidential Action:

-

Title:

[NCHS] Research Data Center (RDC) Proposal for Access to Confidential Data for the National Center for Health Statistics

Reference Number:

202506-0920-005

Omb Control Number:

0920-1363

Agency:

HHS/CDC

Received:

2025-06-26

Concluded:

2025-07-29

Action:

Approved without change

Status:

Active

Request Type:

Reinstatement without change of a previously approved collection
[NCHS] Research Data Center (RDC) Proposal for Access to Confidential Data for the National Center for Health Statistics

Key Information

Abstract

Researchers self-select whether they need access to confidential data to answer their research questions. The RDC requires the researcher to complete a research proposal so NCHS understands the research proposed, whether confidential data is available to address the research questions, how the confidential data will be used and what data outputs the researcher needs to satisfy their project.

Federal Register Notices

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

Authorizing Statutes

42 USC 242k(b)(4)
View Law

Presidential Action:

-

Title:

American Time Use Survey

Reference Number:

202504-1220-002

Omb Control Number:

1220-0175

Agency:

DOL/BLS

Received:

2025-06-26

Concluded:

2025-09-29

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
American Time Use Survey

Key Information

Abstract

The American Time Use Survey (ATUS) is the Nation’s only federally administered, continuous survey on time use in the United States. It measures, for example, time spent with children, working, providing eldercare, sleeping or doing leisure activities. In the United States, several existing Federal surveys collect income and wage data for individuals and families, and analysts often use such measures of material prosperity as proxies for quality of life. Time-use data substantially augment these quality-of-life measures. The data also can be used in conjunction with wage data to evaluate the contribution of non-market work to national economies. This enables comparisons of production between nations that have different mixes of market and non-market activities. The ATUS supports the mission of the Bureau of Labor Statistics by providing data on when, where, and how much employed Americans work. Individuals aged 15 and up are selected from a nationally representative sample of households each month for the ATUS.

Federal Register Notices

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

Authorizing Statutes

13 USC 9
View Law
29 USC 1
View Law

Presidential Action:

-

Title:

SF-424, Application for Federal Assistance

Reference Number:

202503-0570-001CF

Omb Control Number:

4040-0004

Agency:

USDA/RBS

Received:

2025-06-26

Concluded:

2025-07-02

Action:

Approved without change

Status:

Active

Request Type:

RCF New
SF-424, Application for Federal Assistance

Key Information

Presidential Action:

-

Title:

[NCEZID] One Health Harmful Algal Bloom System (OHHABS)

Reference Number:

202501-0920-009

Omb Control Number:

0920-1105

Agency:

HHS/CDC

Received:

2025-06-26

Concluded:

2025-08-08

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
[NCEZID] One Health Harmful Algal Bloom System (OHHABS)

Key Information

Abstract

The purpose of OHHABS is 1) to provide a database for routine data collection at the state/territorial level to identify and characterize HAB events, HAB-associated illnesses, and HAB exposures in the United States and 2) to better inform and improve our understanding of HAB-associated illnesses and exposures through routine surveillance to inform public health policy and illness prevention efforts. OHHABS (electronic, year-round collection) includes questions about HAB events and HAB-associated-illness for human and animal cases. OHHABS, a web-based reporting system, is nationally available for state and territorial health departments to voluntarily report information about HAB-associated human and animal cases and HAB events. This revision contains updates to OHHABS that better align with HAB information as we know it today. Changes include modifying questions, streamlining data collection methods, and the separation of the data collection instrument.

SPD-15 Implementation

Yes

Federal Register Notices

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

Authorizing Statutes

42 USC 241
View Law

Presidential Action:

-

Title:

Annual Report for Chief Compliance Officer of Registrants

Reference Number:

202505-3038-002

Omb Control Number:

3038-0080

Agency:

CFTC

Received:

2025-06-26

Concluded:

2025-08-08

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Annual Report for Chief Compliance Officer of Registrants

Key Information

Abstract

On April 3, 2012, the Commission adopted Regulation 3.3 (Chief Compliance Officer) under sections 4d(d) and 4s(k) of the Commodity Exchange Act (“CEA”). Commission Regulation 3.3 requires each futures commission merchant (“FCM”), swap dealer (‘‘SD’’), and major swap participant (“MSP”) to designate, by filing a Form 8–R, a chief compliance officer (“CCO”) who is responsible for: (1) developing and administering each registrant’s policies and procedures that fulfill certainrelating to its business as a duties of the SD, MSP, or FCM and that are reasonably designed to ensure the registrant’s compliance withrequired to be established pursuant to the CEA and Commission regulations; (2) taking reasonable steps to resolve material conflicts of interest relating to the registrant’s business as a SD, MSP, or FCM; (3) taking reasonable steps to ensure compliance with the CEA and Commission regulations relating to the registrant’s business as a SD, MSP, or FCM; (4) taking reasonable steps to ensure the registrant establishes, maintains, and reviews written policies and procedures reasonably designed to remediate establishing procedures for the remediation of noncompliance issues identified by the chief compliance officerCCO; (5) taking reasonable steps to ensure the registrant establishing establishes procedures for the handling, management response, remediation, retesting, and closing of noncompliance issues; (6) preparing, signing, certifying, furnishing to the board of directors, senior officers, and (if applicable) audit committee, and filing with the Commission an annual compliance report that contains the information specified in the regulations Commission regulation 3.3(e; ). Commission regulation 3.3 also requires that SDs, MSPs, and FCMs: (1) amending the annual report if material errors or omissions are identified; and (2) request that the Commission grant an extension of time to furnish the annual report, if failure to timely furnish could not be eliminated without unreasonable effort or expense; and (3) maintaining records of the registrant’s compliance policies and procedures and records related to the annual report. The information collection obligations imposed by Commission Regulation 3.3 are essential to ensuring that FCMs, SDs, and MSPs maintain comprehensive policies and procedures that promote compliance with the CEA and Commission regulations. In particular, the Commission believes that, among other things, these obligations (i) promote compliance behavior through periodic self-evaluation, (ii) inform the Commission of possible compliance weaknesses, (iii) assist the Commission in determining whether the registrant remains in compliance with the CEA and Commission regulations, and (iv) help the Commission to assess whether the registrant has mechanisms in place to adequately address compliance problems that could lead to a failure of the registrant.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 111 - 203 124 Stat. 1376 (2010)
View Law
7 USC 6d(d) and 6s(k)
View Law

Presidential Action:

-

Title:

Reporting, Recordkeeping, and Daily Trading Records Requirements for Swap Dealers and Major Participants.

Reference Number:

202505-3038-003

Omb Control Number:

3038-0087

Agency:

CFTC

Received:

2025-06-26

Concluded:

2025-08-08

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Reporting, Recordkeeping, and Daily Trading Records Requirements for Swap Dealers and Major Participants.

Key Information

Abstract

Section 731 of Title VII of the Dodd-Frank Act amended the Commodity Exchange Act (CEA) to add section 4s(f) and 4s(g) which establish certain reporting, recordkeeping, and daily trading records requirements for swap dealers (SDs) and major swap participants (MSPs). Specifically, section 4s(f) authorizes the Commission to promulgate books and records and reporting requirements for SDs and MSPs. It also expressly obligates SDs and MSPs to maintain records of all activities related to their swaps businesses and to make reports regarding their transactions, positions and financial condition, as required by such regulations. Section 4s(g) requires SDs and MSPs to maintain daily trading records of their swaps that contain any information prescribed by Commission regulations; all related records (including records of related cash and forward transactions); all recorded communications (including electronic mail, instant messages, and recordings of telephone calls); and a complete audit trail for conducting comprehensive and accurate trade reconstruction. Section 4s(g) also requires that the daily trading records for each swap transaction be identifiable by transaction and by counterparty.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 111 - 203 124 Stat. 1376 (2010)
View Law

Presidential Action:

-

Title:

NRC Form 531, Request for Taxpayer Identification Number

Reference Number:

202506-3150-002

Omb Control Number:

3150-0188

Agency:

NRC

Received:

2025-06-26

Concluded:

2025-12-29

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
NRC Form 531, Request for Taxpayer Identification Number

Key Information

Abstract

The Debt Collection Improvement Act of 1996 requires that agencies collect TINs from individuals who do business with the Government, including contractors and recipients of credit, licenses, permits, and benefits. The TIN will be used to process all electronic payments (refunds) made to licensees by electronic funds transfer by the Department of the Treasury. The Department of the Treasury will use the TIN to determine whether the refund can be used to administratively offset any delinquent debts reported to the Treasury by other Government agencies. In addition, the TIN will be used to collect and report to the Department of the Treasury any delinquent indebtedness arising out of the licensee’s or applicant’s relationship with the NRC.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 83 - 703 1-311
View Law
Pub.L. 104 - 134 110 STAT 1321
View Law

Presidential Action:

-

Title:

Incidental Take of Marine Mammals During Specified Activities (50 CFR 18.27 and 50 CFR 18, Subpart L)

Reference Number:

202503-1018-003

Omb Control Number:

1018-0203

Agency:

DOI/FWS

Received:

2025-06-26

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

New collection (Request for a new OMB Control Number)
Incidental Take of Marine Mammals During Specified Activities (50 CFR 18.27 and 50 CFR 18, Subpart L)

Key Information

Abstract

The Marine Mammal Protection Act (MMPA) of 1972, as amended (16 U.S.C. 1361 et seq.) imposed, with certain exceptions, a moratorium on the taking of marine mammals. Section 101(a)(5)(A) of the MMPA directs the Secretary of the Interior (Secretary) to allow, upon request by citizens of the United States, the taking of small numbers of marine mammals incidental to specified activities (other than commercial fishing) if the Secretary makes certain findings and prescribes specific regulations that, among other things, establish permissible methods of taking. Once the U.S. Fish and Wildlife Service (Service or we) issue specific regulations, applicants seeking to conduct activities must request a Letter of Authorization (LOA) for the specific activity and submit onsite monitoring reports and a final report of the activity to the Secretary. Procedural regulations outlining the requirements for the submission of a request are contained in 50 CFR 18.27. We request OMB approval of the specific regulations governing authorized incidental take of marine mammals activities as separate control numbers for each subpart to facilitate simultaneous rulemaking actions when we receive applications for ITR.

Federal Register Notices

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

Authorizing Statutes

16 USC 1361 et seq.
View Law

Presidential Action:

-

Title:

Non-combatant Tracking System (NTS) & Evacuation Tracking and Accountability System (ETAS)

Reference Number:

202505-0704-010

Omb Control Number:

0704-0629

Agency:

DOD/DODDEP

Received:

2025-06-26

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Revision of a currently approved collection
Non-combatant Tracking System (NTS) & Evacuation Tracking and Accountability System (ETAS)

Key Information

Abstract

E.O. 12656 establishes the responsibility for Department of Health and Human Services and Department of Defense (DoD) to take care of any American citizens and family members that are evacuated from any country and ensure their personal needs are met. This information collection is needed to collect the required evacuee information necessary to document the movement of an evacuee from a foreign country to an announced safe haven and to assist the evacuee in meeting their needs, as well as, to ensure that Federal and State agencies receive proper reimbursement for costs incurred.

Federal Register Notices

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

Presidential Action:

-

Title:

[PHIC] Assessment of Outcomes Associated with the Preventive Health and Health Services Block Grant

Reference Number:

202506-0920-016

Omb Control Number:

0920-1257

Agency:

HHS/CDC

Received:

2025-06-25

Concluded:

2025-08-11

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
[PHIC] Assessment of Outcomes Associated with the Preventive Health and Health Services Block Grant

Key Information

Abstract

This data collection will assess select cross-cutting outputs and outcomes of the PHHS Block Grant and demonstrates the utility of the grant on a national level. Respondents include the 61 Block Grant grantees. Data will be collected using a web-based data collection instrument in fall 2019. The previous survey instrument launched in 2022 will be used. No questions have been added or deleted. Prompts were added to the Q5 and Q8 series to reduce errors.Changes to the Healthy People 2030 Topic Area 25 are expected to ensure compliance with Executive Order 14168.

Federal Register Notices

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

Authorizing Statutes

42 USC 241
View Law

Presidential Action:

-

Title:

Statement of a Person Claiming Loan Fee Refund Due a Deceased Veteran, Service Member, or Surviving Spouse (VA Forms 26-10280 and 26-10280a)

Reference Number:

202504-2900-002

Omb Control Number:

2900-0910

Agency:

VA

Received:

2025-06-25

Concluded:

2025-07-28

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Statement of a Person Claiming Loan Fee Refund Due a Deceased Veteran, Service Member, or Surviving Spouse (VA Forms 26-10280 and 26-10280a)

Key Information

Abstract

This information collection seeks to streamline the loan fee refund process through the use of a form that collects information needed for VA to release the refund to an individual other than the Veteran. VA has further determined that it may release the funds directly to the individual, rather than to the estate of the Veteran, provided the person claiming the refund attests to certain information regarding the Veteran’s estate as well as their intention to disburse the refund in accordance with appropriate estate laws. VA notes that this approach is consistent with how other federal agencies, such as the Internal Revenue Service, process refunds owed to deceased individuals.

Federal Register Notices

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

Presidential Action:

-

Title:

Application for Approved Finance Provider

Reference Number:

202506-3048-002

Omb Control Number:

3048-0032

Agency:

EXIMBANK

Received:

2025-06-25

Concluded:

2025-08-08

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Application for Approved Finance Provider

Key Information

Abstract

The application for Approved Finance Provider will be used to determine if the finance provider has the financial strength and administrative staff to originate, administer, collect, and if needed, restructure international loans. The application will also improve EXIM Bank's compliance with the Open Government initiative by providing transparency into specific information used to determine if an applicant is qualified to use our loan guarantee programs. EXIM Bank has made non substantive changes to the form. The purpose of the change is to reflect the requested content fully and clearly in accordance with what the form already requires. No additional burden or change in user experience will result.

Federal Register Notices

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

Authorizing Statutes

12 USC 635
View Law

Presidential Action:

-

Title:

Generic Clearance for Usability Data Collections

Reference Number:

202506-0693-001

Omb Control Number:

0693-0043

Agency:

DOC/NIST

Received:

2025-06-25

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Extension without change of a currently approved collection
Generic Clearance for Usability Data Collections

Key Information

Abstract

NIST proposes to conduct a number of data collection efforts - both quantitative and qualitative. The data collections will be designed to evaluate the usability and utility of NIST research for measurement and standardization work. These data collection efforts may include, but may not be limited to electronic methodologies, empirical studies, video and audio collections, interview and questionnaires.

Federal Register Notices

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

Presidential Action:

-

Title:

FDA Adverse Event and Product Experience Reporting Systems (MEDWATCH and SPS electronic and paper-based collection)

Reference Number:

202411-0910-004

Omb Control Number:

0910-0291

Agency:

HHS/FDA

Received:

2025-06-25

Concluded:

2025-09-15

Action:

Approved with change

Status:

Active

Request Type:

Revision of a currently approved collection
FDA Adverse Event and Product Experience Reporting Systems (MEDWATCH and SPS electronic and paper-based collection)

Key Information

Abstract

This information collection supports implementation of FDA's adverse event reporting programs, including voluntary reports as well as reports utilizing paper-based submission. Respondents to the collection are those who submit event experience information to the agency regarding products regulated by FDA.

Federal Register Notices

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

Authorizing Statutes

21 USC 301 et seq.
View Law

Presidential Action:

-

Title:

[NCCDPHP] National Program of Cancer Registries Program Evaluation Instrument

Reference Number:

202506-0920-012

Omb Control Number:

0920-0706

Agency:

HHS/CDC

Received:

2025-06-25

Concluded:

2025-08-11

Action:

Approved without change

Status:

Active

Request Type:

Reinstatement with change of a previously approved collection
[NCCDPHP] National Program of Cancer Registries Program Evaluation Instrument

Key Information

Abstract

This Reinstatement with Change of a previously approved collection request is to reinstate the NPCR-PEI process and update the survey instrument based on feedback from stakeholders and revisions to NPCR Program Standards. CDC requests a three-year clearance for the proposed program evaluation instrument. Content of the NPCR PEI instrument is updated based on feedback from stakeholders and updates to NPCR Program Standards. A determination was made to edit and clarify various questions; some questions were deleted or revised because they were no longer relevant; no new questions were proposed based on the need for information from awardees to CSB and FOA DP22-2202 requirements.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 102 - 515 3312
View Law
42 USC 301
View Law

Presidential Action:

-

Title:

Emergency Cruise Ship Outbreak Investigations (CSOIs)

Reference Number:

202503-0920-010

Omb Control Number:

0920-1255

Agency:

HHS/CDC

Received:

2025-06-25

Concluded:

None

Action:

None

Status:

Received in OIRA

Request Type:

Reinstatement with change of a previously approved collection
Emergency Cruise Ship Outbreak Investigations (CSOIs)

Key Information

Abstract

The purpose of this data collection is to allow CDC to conduct emergency cruise ship outbreak investigations (CSOIs) of acute gastroenteritis (AGE) outbreaks or when unusual AGE illness clusters occur. The Vessel Sanitation Program (VSP) deploys to the field and conducts CSOIs to assist cruise industry partners as they respond to AGE outbreaks or events on their vessels. Under this generic clearance, CDC will seek emergency PRA clearance for each CSOI within 24-hours of submission to OMB. The data collection period for each CSOI will not exceed 30 days. Data will be gathered by NCEH's VSP. Submission of Revision ICR for 0920-1255 is submitted for approval of Generic mechanism for an additional three years and a reduction in burden hours (4,063 annually) due to the refinement in estimated number of CSOIs conducted annually in response to cruise ship AGE outbreaks.

Federal Register Notices

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

Authorizing Statutes

42 USC 269
View Law
42 USC Part 71
View Law
42 USC 264
View Law

Presidential Action:

-

Title:

Administrative Detention and Banned Medical Devices

Reference Number:

202410-0910-003

Omb Control Number:

0910-0114

Agency:

HHS/FDA

Received:

2025-06-25

Concluded:

2025-09-16

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Administrative Detention and Banned Medical Devices

Key Information

Abstract

The FDA has the statutory authority under section 304(g) of the FD&C Act to detain devices during establishment inspections which are believed to be adulturated or misbranded. On March 9, 1979, FDA issued a final regulation on Administrative Detention Procedures which includes, among other things, certain reporting and recordkeeping requirements. FDA also has the statutory authority under section 516 of the Act to ban devices that present substantial deception, unreasonable and substantial risk of illness or injury, or unreasonable, direct and substantial danger to the health of individuals. Under these authorities there are requirements pertaining to reporting and recordkeeping activities that are necessary in order for the Agency to carry out its mission to protect the public health.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

21 USC 334(g)
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Presidential Action:

-

Title:

Sections 63.01, 63.03, and 63.04, Procedures for Applicants Requiring Section 214 Authorization for Domestic Interstate Transmission Lines Acquired Through Corporate Control

Reference Number:

202505-3060-031

Omb Control Number:

3060-0989

Agency:

FCC

Received:

2025-06-25

Concluded:

2025-06-25

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Sections 63.01, 63.03, and 63.04, Procedures for Applicants Requiring Section 214 Authorization for Domestic Interstate Transmission Lines Acquired Through Corporate Control

Key Information

Abstract

All telecommunications carriers seeking domestic section 214 approval concerning acquisitions of corporate control are required to comply with 47 CFR sections 63.03 and 63.04 of the Commission's rules. In this information collection, there are two requirements identified, i.e., filing procedures for domestic transfer of control applications and pro forma transactions. The information will be used to ensure that applicants comply with the requirements of 47 USC section 214.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

47 USC 152,154(i)-(j),201,214,303(r)
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Presidential Action:

-

Title:

Notice of Rescission of Coverage and Disclosure Requirements for Patient Protection under the Affordable Care Act (CMS-10330)

Reference Number:

202506-0938-012

Omb Control Number:

0938-1094

Agency:

HHS/CMS

Received:

2025-06-25

Concluded:

2025-12-22

Action:

Approved without change

Status:

Active

Request Type:

Reinstatement without change of a previously approved collection
Notice of Rescission of Coverage and Disclosure Requirements for Patient Protection under the Affordable Care Act (CMS-10330)

Key Information

Abstract

Sections 2712 and 2719A of the Public Health Service Act (PHS Act), as added by the Affordable Care Act, contain rescission notice, and patient protection disclosure requirements that are subject to the Paperwork Reduction Act of 1995. The No Surprises Act, enacted as part of the Consolidated Appropriations Act, 2021, amended section 2719A of the PHS Act to sunset when the new emergency services protections under the No Surprises Act take effect. The provisions of section 2719A of the PHS Act will no longer apply with respect to plan years beginning on or after January 1, 2022. The No Surprises Act re-codified the patient protections related to choice of health care professional under section 2719A of the PHS Act in newly added section 9822 of the Internal Revenue Code, section 722 of the Employee Retirement Income Security Act, and section 2799A-7 of the PHS Act and extended the applicability of these provisions to grandfathered health plans for plan years beginning on or after January 1, 2022. The rescission notice will be used by health plans to provide advance notice to certain individuals that their coverage may be rescinded as a result of fraud or intentional misrepresentation of material fact. The patient protection notification will be used by health plans to inform certain individuals of their right to choose a primary care provider or pediatrician and to use obstetrical/gynecological services without prior authorization. The related provisions are finalized in the 2015 final regulations titled “Final Rules under the Affordable Care Act for Grandfathered Plans, Preexisting Condition Exclusions, Lifetime and Annual Limits, Rescissions, Dependent Coverage, Appeals, and Patient Protections” (80 FR 72192, November 18, 2015) and 2021 interim final regulations titled “Requirements Related to Surprise Billing; Part I”. The 2015 final regulations also require that, if State law prohibits balance billing, or a plan or issuer is contractually responsible for any amounts balanced billed by an out-of-network emergency services provider, a plan or issuer must provide a participant, beneficiary or enrollee adequate and prominent notice of their lack of financial responsibility with respect to amounts balanced billed in order to prevent inadvertent payment by the individual. Plans and issuers will not be required to provide this notice for plan years beginning on or after January 1, 2022.

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

Pub.L. 111 - 148 2711
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Pub.L. 111 - 148 2712 86 FR 36872
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Pub.L. 111 - 148 2719A
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Presidential Action:

-

Title:

Transportation of Household Goods; Consumer Protection

Reference Number:

202504-2126-001

Omb Control Number:

2126-0025

Agency:

DOT/FMCSA

Received:

2025-06-25

Concluded:

2026-01-12

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Transportation of Household Goods; Consumer Protection

Key Information

Abstract

This is an ICR renewal. The collections in this ICR are mandatory and consists mostly of recordkeeping and disclosure, where a motor carrier provides information when a consumer requests that a mover provide an estimate and when a consumer decides to have a particular mover transport household goods. Certain information will be transferred to the consumer for the consumer to educate himself/herself of his/her rights and responsibilities in commercial transactions with the mover. FMCSA has the authority to regulate the operations of the household goods industry. Under 49 U.S.C. § 14104(a)(1), paperwork required of household goods motor carriers must be minimized to the maximum extent feasible, consistent with the protection of individual shippers. This ICR includes the information collection requirements contained in 49 CFR part 375, Transportation of Household Goods in Interstate Commerce; Consumer Protection Regulations. FMCSA will use the information provided by the shippers, when necessary, while conducting reviews, audits and investigations of carriers to determine if a carrier/mover is in compliance with the Federal requirements. If this collected information were not available, FMCSA would have no means of independently verifying compliance. The collected information will assist consumers in their commercial dealings with interstate motor carriers by enabling them to receive consumer protection materials electronically. FMCSA will use the information provided by the shippers, when necessary, while conducting reviews, audits and investigations of carriers to determine if a carrier/mover is in compliance with the Federal requirements. If this collected information were not available, FMCSA will have no means of independently verifying compliance. The frequency of the collection varies and is based on the number of moves and requests made, based on shippers needs, and is not a factor FMCSA or the carrier can control. The information is not collected more frequently than quarterly since the data is required only when services are requested by the consumer. This is to help the consumer understand each part of the commercial transaction and determine whether they are being defrauded or deceived by a mover. This supporting statement divides the burden into five collections roughly corresponding to the subsections in the HHG regulations in which the specific paperwork and record keeping requirements for HHG movers appear: • IC-1: Required Information for Prospective Individual Shippers • IC-2: Estimating Charges • IC-3: Pick Up of Shipments of Household Goods • IC-4: Transportation of Shipments • IC-5: Consumer Complaints

Federal Register Notices

60-Day FRN
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30-Day FRN
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Authorizing Statutes

Pub.L. 109 - 59 4205, 119 Stat. 1144, 1751
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Presidential Action:

-
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