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.

Full Inventory
Under Review
Presidential Action Driven

Showing 25 of 15120 results

CSV Download

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

Title:

Ambulatory Surgical Center Quality Reporting Program (CMS-10530)

Reference Number:

202412-0938-019

Omb Control Number:

0938-1270

Agency:

HHS/CMS

Received:

2025-01-10

Concluded:

2025-07-29

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Ambulatory Surgical Center Quality Reporting Program (CMS-10530)

Key Information

Abstract

Section 109(a) of the Tax Relief and Health Care Act of 2006 (TRHCA) (Pub. L. 109-432) amended section 1833(t) of the Social Security Act by adding a new subsection (17) that affects the payment rate update applicable to Outpatient Prospective Payment System (OPPS) payments for services furnished by hospitals in outpatient settings on or after January 1, 2009. Section 1833(t)(17)(A) of the Social Security Act, which applies to hospitals as defined under section 1886(d)(1)(B) of the Social Security Act, requires that hospitals that fail to report data required for quality measures selected by the Secretary in the form and manner required by the Secretary under section 1833(t)(17)(B) of the Social Security Act will incur a reduction in their annual payment update (APU) factor to the hospital outpatient department fee schedule by 2.0 percentage points. Hospital OQR Program payment determinations are made based on Hospital OQR Program quality measure data reported and supporting forms submitted by hospitals as specified through rulemaking. To reduce burden, a variety of different data collection mechanisms are employed, with every consideration taken to employ existing data and data collection systems.

Federal Register Notices

60-Day FRN
View Notice

Authorizing Statutes

Pub.L. 109 - 432 109(b)
View Law
42 USC 1395
View Law

Presidential Action:

-

Title:

Rural Emergency Hospital Quality Reporting (REHQR) (CMS-10870)

Reference Number:

202412-0938-021

Omb Control Number:

0938-1454

Agency:

HHS/CMS

Received:

2025-01-10

Concluded:

2025-07-28

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Rural Emergency Hospital Quality Reporting (REHQR) (CMS-10870)

Key Information

Abstract

The Consolidated Appropriations Act (CAA), 2021, was signed into law in December 2020. In this legislation, Congress established a new Medicare provider type: Rural Emergency Hospitals (REHs). Section 125 of Division CC of the CAA, 2021 added section 1861(kkk) to the Social Security Act (the Act). This section defines an REH as a facility that, in relevant part, was as of December 27, 2020: (1) a Critical Access Hospital (CAH) or a subsection (d) hospital with not more than 50 beds located in a county (or equivalent unit of local government) in a rural area (defined in section 1886(d)(2)(D) of the Act); or (2) was a subsection (d) hospital with not more than 50 beds that was treated as being in a rural area pursuant to section 1886(d)(8)(E) of the Act. Under section 1861(kkk)(7) of the Act, as added by section 125 of Division CC of the CAA, 2021, the Secretary is required to establish quality measurement reporting requirements for REHs, which may include the use of a small number of claims-based measures or patient experience surveys. An REH must submit quality measure data to the Secretary, and the Secretary shall establish procedures to make the data available to the public on a CMS website.

Federal Register Notices

60-Day FRN
View Notice

Authorizing Statutes

42 USC 1395x
View Law
Pub.L. 116 - 260 125
View Law

Presidential Action:

-

Title:

Medical Qualification Requirements

Reference Number:

202411-2126-002

Omb Control Number:

2126-0006

Agency:

DOT/FMCSA

Received:

2025-01-08

Concluded:

2025-03-25

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Medical Qualification Requirements

Key Information

Abstract

This request for renewal provides an increase from the previously approved annual burden hours as a result of updated driver and motor carrier population information, program statistics, National Registry statistics, and wage data. The information collection requirements are mandatory and apply to drivers, motor carriers, MEs, ME applicant testing organizations, and TCs. IC-1: Physical Qualification Standards; MEs must provide driver medical exam information for drivers they examine on medical forms and in the National Registry. The ME can determine if the driver is medically qualified. The ME must complete and furnish the original paper MEC to the driver. The driver must complete driver health history portion of the MER Form at least every 2 years. The motor carrier must file a MEC in DQ record. IC-2: Resolution of Medical Conflict; The medical conflict application provision provides a mechanism for drivers and motor carriers to request FMCSA to make a final decision to resolve conflicting medical evaluations when either party does not accept the decision of a medical specialist. FMCSA uses the information to determine if the driver should or should not be qualified. Motor carriers are required to submit an application to FMCSA for resolution (up to 3 cases a year) and attend a hearing (1 per year) if FMCSA deems necessary. IC-3: Medical Exemptions; FMCSA may grant a vision, hearing, or seizure exemption from a physical qualification standard. The driver is to complete an application for new exemption and exemption renewal every 2 years and the motor carrier is to copy and file the exemption in the DQ file. IC4: Skill Performance Evaluation Certificate; The SPE Certificate program requires drivers to complete an application for the new SPE certificate, complete an application for SPE certificate renewal every 2 years, provide a copy of the MER Form and MEC to FMCSA, and for motor carriers to copy and file the SPE Certificate in the DQ record. IC-5: National Registry of Certified Medical Examiners; MEs are required to provide contact and employment data when registering to become a certified ME. This data is used to provide the public with contact information for those medical professionals who are certified by FMCSA to conduct interstate CMV driver medical exams. MEs are required to submit the results of each CMV driver medical exam they complete daily, copies of MER forms, and MECs via the National Registry. IC-6: Medical Examiner’s Certification Integration Final Rule; Beginning on June 23, 2025, MEs will no longer be required to complete and furnish the original written MEC to qualified drivers when the driver is a CDL/CLP holder. This information will be electronically transmitted to the SDLA. Employers will no longer need to request a copy of the handwritten MEC for CDL/CLP holders. In addition, employers will no longer be required to verify the ME’s National Registry number for MECs issued to CDL/CLP holders because only MEs listed on the National Registry will be able to forward MEC information to the National Registry. IC-7: Qualifications of Drivers; Diabetes Standard; An individual with ITDM is able to obtain an MEC from an ME for up to a maximum of 12 months if the TC, the healthcare professional who manages, and prescribes insulin for the treatment of the individual’s diabetes, attests to the ME the individual maintains a stable insulin regimen and proper control of diabetes, and the ME determines the individual meets FMCSA’s physical qualification standards. The information provided by the TC enables the ME to make a qualification determination based on whether the driver meets all the physical qualification requirements.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 109 - 59 4116
View Law
Pub.L. 109 - 59 4129
View Law

Presidential Action:

-

Title:

Application for Registration-DEA 224, Application of Registration Renewal-DEA 224A

Reference Number:

202410-1117-001

Omb Control Number:

1117-0014

Agency:

DOJ/DEA

Received:

2025-01-08

Concluded:

2025-04-11

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Application for Registration-DEA 224, Application of Registration Renewal-DEA 224A

Key Information

Abstract

The DEA implements and enforces titles II and III of the Comprehensive Drug Abuse Prevention and Control Act of 1970, Pub. L. No. 91-513, 84 Stat. 1242 (1970), as amended (the “CSA”). 21 U.S.C. 801–971. Through the enactment of the CSA and its amendments, Congress established a closed system of distribution making it unlawful to handle any controlled substance except in a manner authorized by the CSA. In order to maintain this closed system of distribution, the CSA generally requires all persons who handle controlled substances to obtain a registration issued by the Attorney General. 21 U.S.C. 822, 823, 957, and 958.

Federal Register Notices

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

Authorizing Statutes

21 USC 822
View Law
21 USC 823
View Law
Pub.L. 91 - 513 1242
View Law

Presidential Action:

-

Title:

Emergency Medical Services Recordkeeping and Notice Requirements (No Form)

Reference Number:

202410-1117-002

Omb Control Number:

1117-0060

Agency:

DOJ/DEA

Received:

2025-01-08

Concluded:

2025-04-11

Action:

Approved without change

Status:

Active

Request Type:

New collection (Request for a new OMB Control Number)
Emergency Medical Services Recordkeeping and Notice Requirements (No Form)

Key Information

Abstract

The Drug Enforcement Administration (DEA) seeks approval by the Office of Management and Budget (OMB) for a new collection of information, Emergency Medical Services and Recordkeeping and Notice Requirements. This information collection request is associated with DEA’s “Registering Emergency Medical Services Agencies under the Protecting Patient Access to Emergency Medications Act of 2017” rulemaking, RIN 1117-AB37.

Federal Register Notices

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

Authorizing Statutes

21 USC 823j
View Law

Presidential Action:

-

Title:

Section 73.3588, Dismissal of Petitions to Deny or Withdrawal of Informal Objections

Reference Number:

202501-3060-004

Omb Control Number:

3060-0423

Agency:

FCC

Received:

2025-01-08

Concluded:

2025-01-08

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Section 73.3588, Dismissal of Petitions to Deny or Withdrawal of Informal Objections

Key Information

Abstract

To ensure that petition to deny was filed under appropriate circumstances and not to extract payment in excess of legitimate and prudent expenses. Section 73.3588 requires the filing party to obtain approval from the FCC to dismiss or withdraw its petition to deny by filing a request for approval of the dismissal or withdrawal, a copy of any written agreement, an affidavit stating that the petitioner has not received any consideration in excess of legitimate and prudent expenses in exchange for the dismissal or withdrawal, and an itemization of the expenses for which it is seeking reimbursement.

Federal Register Notices

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

Authorizing Statutes

47 USC 154(i)
View Law

Presidential Action:

-

Title:

Joint Outpatient Experience Survey (JOES)

Reference Number:

202501-0720-001

Omb Control Number:

0720-0085

Agency:

DOD/DODOASHA

Received:

2025-01-08

Concluded:

2025-01-08

Action:

Approved without change

Status:

Active

Request Type:

New collection (Request for a new OMB Control Number)
Joint Outpatient Experience Survey (JOES)

Key Information

Abstract

The core objective of the JOES Survey Suite is to systematically assess MHS beneficiaries' perceptions of their outpatient care quality when received directly at Military Treatment Facilities (MTFs) and through civilian network providers reimbursed by the MHS (private sector care). The JOES Survey Suite collects feedback from military personnel, military family members, and retirees regarding their outpatient care. These surveys gather insights into beneficiaries' perspectives on the care they received during outpatient visits in order to identify opportunities to improve the care provided by MHS providers and systems.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 114 - 92 713 Expansion of Evaluation
View Law
Pub.L. 102 - 484 724 Annual Healthcare Survey
View Law

Presidential Action:

-

Title:

Personnel Vetting Questionnaire (PVQ)

Reference Number:

202409-7100-001CF

Omb Control Number:

3206-0279

Agency:

FRS

Received:

2025-01-08

Concluded:

2025-01-08

Action:

Approved without change

Status:

Active

Request Type:

RCF New
Personnel Vetting Questionnaire (PVQ)

Key Information

Presidential Action:

-

Title:

H-2 Petitioner's Employment Related or Fee Related Notification

Reference Number:

202412-1615-002

Omb Control Number:

1615-0107

Agency:

DHS/USCIS

Received:

2025-01-08

Concluded:

2025-01-14

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
H-2 Petitioner's Employment Related or Fee Related Notification

Key Information

Abstract

USCIS requires H-2 petitioners to notify USCIS when (1) a worker fails to report to work within 5 workdays of the employment start date listed on the petition; (2) the labor or services for which H-2 workers were hired is completed more than 30 days early; (3) a worker leaves the worksite without notice; or (4) a worker is terminated prior to the completion of the labor or services for which the worker was hired. The notification requirement is necessary to ensure that H-2 workers maintain their nonimmigrant status and helps prevent H-2 workers from engaging in unauthorized employment. The information collected in employment-related notification submitted by H-2 petitioners is used by USCIS, U.S. Customs and Border Protection (CBP), and U.S. Immigration and Customs Enforcement (ICE). USCIS may forward relevant information to both ICE and CBP. ICE uses the information for future adjudicative purposes and CBP uses it to collect all liquidated damage payments from H-2 petitioners. Establishing compliance with this notification requirement is also a condition of H-2A petitioners being able to request substitutions for H-2A workers who have been admitted to the U.S according to 8 CFR 214.2(h)(5)(ix).

Federal Register Notices

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

Authorizing Statutes

8 USC 1184
View Law

Presidential Action:

-

Title:

Implementation of the Violence Against Women Reauthorization Act of 2013

Reference Number:

202501-2577-002

Omb Control Number:

2577-0286

Agency:

HUD/PIH

Received:

2025-01-08

Concluded:

2025-01-10

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Implementation of the Violence Against Women Reauthorization Act of 2013

Key Information

Abstract

The Violence Against Women Reauthorization Act of 2013 (“VAWA”) protects qualified tenants, participants, applicants, and affiliated individuals in all HUD-covered housing programs, who are victims of domestic violence, dating violence, sexual assault, or stalking. On November 16, 2016, HUD published a final rule (VAWA Rule) at 81 FR 80724, implementing VAWA’s provisions in its housing programs. The VAWA Rule includes the following Appendices, which entail certain reporting and recordkeeping burdens: (A) Notice of Occupancy Rights Under the Violence Against Women Act; (B) Model Emergency Transfer Plan for Victims of Domestic Violence, Dating Violence, Sexual Assault, or Stalking; (C) Certification of Domestic Violence, Dating Violence, Sexual Assault, or Stalking, and Alternate Documentation; and (D) Emergency Transfer Request for Certain Victims of Domestic Violence, Dating Violence, Sexual Assault, or Stalking. Under the VAWA Rule, PHAs, owners, and managers (collectively “Covered Housing Providers” or “CHPs”) Under the VAWA Rule, each CHP must make use of Appendix A and Appendix C, by providing copies of the Notice of Occupancy Rights and the Certification form. Each CHP presented with a claim for continued or initial tenancy or assistance, based on the victim’s status as a victim of domestic violence, dating violence, sexual assault, or stalking, may request that the victim document or provide written evidence to demonstrate that the violence occurred, and Certification form is one such way of documenting the violence. Each CHP must also establish an emergency transfer plan, although it need not be modeled on Appendix B. CHPs’ use of an Emergency Transfer Request form, like the model in Appendix D, is also discretionary. CHPs must track and report annually to HUD if they have any Emergency Transfer Requests and outcomes. Finally, under the VAWA Rule, CHPs may opt to provide a lease bifurcation to VAWA-covered individuals.

Federal Register Notices

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

Presidential Action:

-

Title:

Disability Report - Adult

Reference Number:

202501-0960-002

Omb Control Number:

0960-0579

Agency:

SSA

Received:

2025-01-08

Concluded:

2025-02-27

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Disability Report - Adult

Key Information

Abstract

State Disability Determination Services (DDS) use Form SSA-3368, Disability Report – Adult, and its electronic versions, to determine if an adult disability applicant’s impairment(s) is severe and, if so, how the impairment(s) affects the applicant’s ability to work. This determination dictates whether the DDS and SSA will find the applicant disabled. The information we collect on the SSA 3368 is used by the State Disability Determination Services (DDS) to obtain evidence and evaluate whether or not an individual is found disabled. The collection is mandatory for applicants filing to obtain Title II disability benefits or Title XVI Supplemental Security Income (SSI) payments. We collect this information from the individual one time. We collect the information via several modalities: the SSA-3368-BK PDF paper form, the EDCS SSA-3368 Intranet application, and the i3368 Internet application. The respondents complete the SSA-3368 by themselves with self help information available, or another may complete the paper form or electronic application on their behalf. The respondents generally do not need information from someone else to complete the application. The respondents are disability applicants or third parties assisting the applicants applying for Title II disability benefits or Title XVI SSI payments. We are submitting a non-substantive Change Request to revise the informational langauge on the save and exit screens for the Internet modallity, i3368.

Federal Register Notices

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

Authorizing Statutes

42 USC 205(a)
View Law
42 USC 223(d)(5)(A)
View Law
42 USC 1631(e)(1)
View Law
42 USC 1631(d)(1)
View Law

Presidential Action:

-

Title:

Sections 74.1203(a)(3), Interference, and 74.1204(f), Protection of FM broadcast, FM Translator and LP100 stations

Reference Number:

202501-3060-005

Omb Control Number:

3060-1263

Agency:

FCC

Received:

2025-01-08

Concluded:

2025-01-08

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Sections 74.1203(a)(3), Interference, and 74.1204(f), Protection of FM broadcast, FM Translator and LP100 stations

Key Information

Abstract

On May 9, 2019, the Commission adopted a Report and Order, Amendment of Part 74 of the Commission’s Rules Regarding FM Translator Interference, FCC 19-40, MB Docket No. 18-119, adopting proposals to streamline the rules relating to interference caused by FM translators and to expedite the translator interference complaint resolution process. These measures are designed to limit or avoid protracted and contentious interference disputes, provide translator licensees additional investment certainty and flexibility to remediate interference, and provide affected stations earlier and expedited resolution of interference complaints. Under this new information collection, the following information collection requirements require OMB approval. Specifically, the FM Translator Interference Report and Order pertains to this new Information Collection as it codifies the translator interference listener complaint requirements under section 74.1201(k) and sections 74.1203(a)(3) (actual interference) and 74.1204(f) (predicted interference) of the rules. The Commission defines the requirements for a listener complaint submitted with a translator interference claim in section 74.1201(k) as a complaint that is signed and dated by the listener and contains the following information: (1) the complainant’s full name, address, and phone number; (2) a clear, concise, and accurate description of the location where the interference is alleged or predicted to occur; (3) a statement that the complainant listens to the desired station using an over-the-air signal at least twice a month, to demonstrate the complainant is a regular listener; and (4) a statement that the complainant has no legal, employment, financial, or familial affiliation or relationship with the desired station, to demonstrate the complainant is disinterested. Electronic signatures are acceptable for this purpose. The FM Translator Interference Report and Order establishes a minimum number of listener complaints, ranging from 6 to 25, depending on the population served within the protected contour of the complaining station. The Commission explains that a proportionate approach, which was supported by multiple commenters, would be fairer and more effective than a single minimum number for all complaining stations. In addition to the required minimum number of valid listener complaints, a station submitting a translator interference claim package pursuant to either section 74.1203(a)(3) or 74.1204(f) must include: (1) a map plotting the specific locations of the alleged interference in relation to the 45 dBu contour of the complaining station; (2) a statement that the complaining station is operating within its licensed parameters; (3) a statement that the complaining station licensee has used commercially reasonable efforts to inform the relevant translator licensee of the claimed interference and attempted private resolution; and (4) U/D data demonstrating that at each listener location the ratio of undesired to desired signal strength exceeds -20 dB for co-channel situations, -6 dB for first-adjacent channel situations or 40 dB for second- or third-adjacent channel situations, calculated using the Commission’s standard contour prediction methodology set out in section 73.313. In the FM Translator Interference Report and Order, the Commission outlines two paths for resolving interference if the translator decides to continue operation on its original channel. First, a translator operator may resolve each listener complaint by working with a willing listener to resolve reception issues. The translator operator must then document and certify that the desired station can now be heard on the listener’s receiver, i.e., that the adjustment to or replacement of the listener’s receiving equipment actually resolved the interference.

Federal Register Notices

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

Authorizing Statutes

47 USC 307, 308, 309, 316, 319
View Law
47 USC 151, 154(i) and (j), 301, 303,
View Law

Presidential Action:

-

Title:

Color-of-Title Application (43 CFR Subparts 2540 and 2541)

Reference Number:

202412-1004-001

Omb Control Number:

1004-0029

Agency:

DOI/BLM

Received:

2025-01-08

Concluded:

2025-12-30

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
Color-of-Title Application (43 CFR Subparts 2540 and 2541)

Key Information

Abstract

The Bureau of Land Management (BLM) collects and uses the information to determine the validity of a claim under the Color-of-Title Act. The following forms comprise an application in support of a Color-of-Title claim: (a) 2540-1, Color-of-Title Application; (b) 2540-2, Conveyances Affecting Color or Claim of Title; and (c) 2540-3, Color-of-Title Tax Levy and Payment Record. A respondent must submit all of the forms concurrently, or the BLM will reject a claim as insufficient. This request is for OMB to renew for this OMB control number for an additional three years.

Federal Register Notices

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

Authorizing Statutes

43 USC 1068, 1068a, 1068b
View Law

Presidential Action:

-

Title:

Prescription Drug Advertisements and Product Communications

Reference Number:

202501-0910-004

Omb Control Number:

0910-0686

Agency:

HHS/FDA

Received:

2025-01-07

Concluded:

2025-07-29

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Prescription Drug Advertisements and Product Communications

Key Information

Abstract

This information collection supports implementation of statutory and regulatory requirements that govern prescription drug advertisements.

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:

United States Gift (and Generation-Skipping Transfer) Tax Return

Reference Number:

202412-1545-014

Omb Control Number:

1545-0020

Agency:

TREAS/IRS

Received:

2025-01-07

Concluded:

2025-04-10

Action:

Approved with change

Status:

Active

Request Type:

Revision of a currently approved collection
United States Gift (and Generation-Skipping Transfer) Tax Return

Key Information

Abstract

Form 709 is used by individuals to report transfers subject to the gift and generation-skipping transfer taxes and to compute these taxes. The IRS uses the information to collect and enforce these taxes, to verify that the taxes are properly computed, and to compute the tax base for the estate tax. Form 709-NA is used to report certain transfers by a nonresident not a citizen of the United States that are subject to the federal gift tax and certain generation-skipping transfer (GST) taxes and to figure the tax due, if any, on those transfers. The Form 709-NA is also used to allocate the lifetime GST exemption to property transferred during a transferor’s lifetime.

Federal Register Notices

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

Authorizing Statutes

26 USC 6075
View Law
26 USC 6019
View Law

Presidential Action:

-

Title:

Department of Labor Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery

Reference Number:

202501-1225-001

Omb Control Number:

1225-0088

Agency:

DOL/DM

Received:

2025-01-07

Concluded:

2025-01-10

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Department of Labor Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery

Key Information

Abstract

This collection of information is necessary to enable the Agency to collect customer and stakeholder feedback in an efficient, timely manner, in accordance with our commitment to improving service delivery. The information collected from our customers and stakeholders will help ensure that users have an effective, efficient, and satisfying experience with the Agency's programs.

Federal Register Notices

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

Presidential Action:

-

Title:

Summary Plan Description Requirements Under the Employee Retirement Income Security Act of 1974, as Amended

Reference Number:

202501-1210-001

Omb Control Number:

1210-0039

Agency:

DOL/EBSA

Received:

2025-01-07

Concluded:

2025-01-13

Action:

Approved without change

Status:

Active

Request Type:

No material or nonsubstantive change to a currently approved collection
Summary Plan Description Requirements Under the Employee Retirement Income Security Act of 1974, as Amended

Key Information

Abstract

The Department has promulgated regulations governing the content and furnishing of SPDs, SMMs, and SMRs at 29 CFR 102-2 (Style and Format of Summary Plan Descriptions); 29 CFR 2520.102-3 (Contents of Summary Plan Descriptions); 29 CFR 2520.102-4 (Option for Different Summary Plan Descriptions); 29 CFR 2520.2520.104b-1 (Disclosure); 29 CFR 2520.104b-2 (Summary Plan Descriptions); 29 CFR 104b-3 (Summary of Material Modifications to the Plan and Changes in the Information Required to be Included in the Summary Plan Description); and 29 CFR 104(b)-(4) (Alternative Methods of Compliance for Furnishing the Summary Plan Description and Summaries of Material Modifications of a Pension Plan to a Retired Participant, a Separated Participant, and a Beneficiary Receiving Benefits). These regulations set standards for the content of these disclosure documents, the methods of furnishing that will satisfy the statutory disclosure requirements, and alternative methods of compliance. In particular, regulations at 29 CFR 2520.104b-1(c) specifically describe the circumstances under which the administrator of an employee benefit plan may furnish required disclosure documents, including the SPD/SMM/SMR, through electronic media. The Department's regulations contain information collections that constitute mandatory third-party disclosure requirements applicable to the majority of Employee Retirement Income Security Act (ERISA)-covered pension and welfare benefit plans. The Department has determined that these information collections are necessary in order to ensure the participants and beneficiaries in employee benefit plans covered under ERISA receive adequate information about the benefits due to them and their rights under the plans.

Federal Register Notices

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

Authorizing Statutes

29 USC 1022
View Law
29 USC 1024
View Law

Presidential Action:

-

Title:

SCORE Culture and Engagement Survey

Reference Number:

202411-0720-001

Omb Control Number:

-

Agency:

DOD/DODOASHA

Received:

2025-01-07

Concluded:

2025-04-24

Action:

Withdrawn

Status:

Historical Inactive

Request Type:

New collection (Request for a new OMB Control Number)
SCORE Culture and Engagement Survey

Key Information

Abstract

The SCORE™ Culture and Engagement Survey (Safety, Communication, Operational Risk, Resiliency/Burnout, and Engagement) is a validated, evidence-based, and outcomes-predictive assessment tool for culture and engagement. With SCORE™ the Defense Health Agency (DHA) Defense Health Network National Capital Region (DHN NCR) can measure, analyze, and respond to current culture, system, and engagement indicators to get a clear picture of our organizational dynamics down to the local level.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 106 - 398 754
View Law

Presidential Action:

-

Title:

Consolidated Vehicle Owner's Manual Requirements for Motor Vehicles and Motor Vehicle Equipment

Reference Number:

202412-2127-007

Omb Control Number:

2127-0541

Agency:

DOT/NHTSA

Received:

2025-01-07

Concluded:

2025-01-16

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Consolidated Vehicle Owner's Manual Requirements for Motor Vehicles and Motor Vehicle Equipment

Key Information

Abstract

This information collection request (ICR) is for fifteen mandatory and voluntary disclosure requirements for manufacturers of motor vehicles and items of motor vehicle equipment. NHTSA has authority to require manufacturers to provide information to first purchasers of motor vehicles or items of motor vehicle equipment related to performance and safety in printed materials that are attached to or accompany the motor vehicle or item of motor vehicle equipment. NHTSA has exercised this authority to require manufacturers to provide certain specified safety information to be readily available to consumers and purchasers of motor vehicles and items of motor vehicle equipment. Some of these requirements are contained in Federal Motor Vehicle Safety Standards (FMVSS) that set performance requirements for motor vehicles and items of motor vehicle equipment. The other requirements are contained in separate regulations. This ICR is a request for reinstatement with modification of a previously approved collection of information pertaining to the requirement to provide certain information to consumers in vehicles’ owner’s manuals that are required to be provided with new motor vehicles. Manufacturers must comply with these requirements whenever they manufacture a vehicle or equipment item that is subject to the requirements. The purpose of the required disclosures is to provide important safety information to vehicle owners. NHTSA is requesting a revision of this collection to include owner’s manual requirements that were established as part of the Seat Belt Reminder System final rule. The revisions to this ICR include the new owner’s manual requirements in 49 CFR Part 571.208. Since NHTSA last requested approval for this ICR, the estimated burden hours have increased by 1,544 hours (8,628 hours to 10,172 hours) and printing costs have increased by $755,040 ($7,971,461 to $8,726,501). The change in burden reflects changes as a result of the rulemaking requiring the development and publication of new information for the owner’s manual. Printing costs have increased due to accounting for the estimated number of vehicles that will be equipped with seat belt reminder systems and will therefore need to comply with the requirements to provide system information and operating instructions.

Federal Register Notices

60-Day FRN
View Notice

Authorizing Statutes

49 USC 30111, 30112, and 30117
View Law

Presidential Action:

-

Title:

Declaration and Signature for Electronic and Magnetic Media Filing

Reference Number:

202412-1545-012

Omb Control Number:

1545-0967

Agency:

TREAS/IRS

Received:

2025-01-07

Concluded:

2025-02-25

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Declaration and Signature for Electronic and Magnetic Media Filing

Key Information

Abstract

The IRS is actively engaged in encouraging e-filing and electronic documentation. The Form 8453 series is used to authenticate the electronically filed tax return, authorize the electronic return originator (ERO) or intermediate service provider (ISP) to transmit the return, and provide the taxpayer's consent to authorize electronic funds withdrawal for payment of taxes owed. Form 8453-WH is used to electronically file Form 1042, Annual Withholding Tax Return for U.S. Source Income of Foreign Persons. Form 8453-EG, E-file Declaration for Forms 709 and 709-NA, is used to authenticate an electronic Form 709 and 709-NA. The Form 8879 series is used authorize the taxpayer and ERO to sign the return using a personal identification number (PIN) and consent to an electronic funds' withdrawal. Form 8879-WH is used to electronically sign Form 1042, Annual Withholding Tax Return for U.S. Source Income of Foreign Persons. Form 8879-EG, E-file Authorization for Forms 709 and 709-NA, is used for electronic signature authorizations for Form 709, or Form 709-NA.

Federal Register Notices

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

Authorizing Statutes

26 USC 6012
View Law
26 USC 6061
View Law

Presidential Action:

-

Title:

The Red Flags Regulations (Under the Fair and Accurate Credit Transactions Act)

Reference Number:

202409-3084-002

Omb Control Number:

3084-0137

Agency:

FTC

Received:

2025-01-07

Concluded:

2025-03-17

Action:

Approved without change

Status:

Active

Request Type:

Extension without change of a currently approved collection
The Red Flags Regulations (Under the Fair and Accurate Credit Transactions Act)

Key Information

Abstract

The Rule implements sections 114 and 315 of the Fair and Accurate Credit Transactions Act of 2003 ("FACT Act"), as amended by the Red Flags Program Clarification Act of 2010. These rules enhance the ability of consumers to resolve problems caused by identity theft and increase the accuracy of consumer reports.

Federal Register Notices

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

Authorizing Statutes

Pub.L. 108 - 159 114, 315
View Law

Presidential Action:

-

Title:

Medical Device Labeling Requirements

Reference Number:

202501-0910-003

Omb Control Number:

0910-0485

Agency:

HHS/FDA

Received:

2025-01-07

Concluded:

2025-07-29

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Medical Device Labeling Requirements

Key Information

Abstract

This ICR collects information from manufacturers, importers, and distributors of medical devices to disclose to health professionals and consumers specific information about themselves or their devices on the label or labeling of their devices. The primary users of the information disclosed on the label or in the labeling of devices are the health professionals who use or prescribe the device or the lay consumers who use the device. The labeling should contain sufficient information for these persons to use the device safely and effectively. FDA may use the information to determine whether there is reasonable assurance of the safety and effectiveness of the device for its intended use.

Federal Register Notices

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

Authorizing Statutes

21 USC 360i(f)
View Law

Presidential Action:

-

Title:

DOL-Only Performance Accountability, Information, and Reporting System

Reference Number:

202411-1205-002

Omb Control Number:

1205-0521

Agency:

DOL/ETA

Received:

2025-01-06

Concluded:

2025-04-23

Action:

Approved with change

Status:

Active

Request Type:

Revision of a currently approved collection
DOL-Only Performance Accountability, Information, and Reporting System

Key Information

Abstract

This request fulfills Workforce Innovation and Opportunity Act reporting requirements regarding the collection of performance indicators described in Sec. 116(b)(2)(A). Requirements for state level collection of this data for the programs contained in this collection are based on WIOA requirements. As part of this ICR, the Department of Labor’s (DOL) Employment and Training Administration (ETA) has made changes to the Participant Individual Record Layout (ETA-9172), (Program) Performance Report (ETA-9173-APPSHP) to facilitate State and grantee performance reporting. In particular, as part of DOL’s effort to streamline program performance reporting for ETA grants with significant apprenticeship components as a primary goal of the program (Apprenticeship grants), DOL is adding the performance information collection requirements for Apprenticeship grants. DOL also is adding a new information collection requirement to this ICR: the Apprenticeship Outreach: Organization/Employer Record Layout.

Federal Register Notices

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

Authorizing Statutes

29 USC 3141(d)
View Law
29 USC 3224
View Law
29 USC 3249
View Law

Presidential Action:

-

Title:

Occupational Safety and Health Onsite Consultation Agreements (29 CFR Part 1908)

Reference Number:

202409-1218-003

Omb Control Number:

1218-0110

Agency:

DOL/OSHA

Received:

2025-01-06

Concluded:

2025-02-24

Action:

Approved without change

Status:

Active

Request Type:

Revision of a currently approved collection
Occupational Safety and Health Onsite Consultation Agreements (29 CFR Part 1908)

Key Information

Abstract

OSHA's On-Site Consultation Service offers free and confidential advice to small and medium-sized businesses in all states across the country, with priority given to high-hazard worksites. Consultation services are totally separate from enforcement and do not result in penalties or citations. The Consultation Program regulations specify services to be provided, and practices and procedures to be followed by the State On-site Consultation Programs. Information collection requirements set forth in the On-site Consultation Program regulations are in two categories: State Responsibilities and Employer Responsibilities. OSHA is proposing to revise the approved Occupational Safety and Health On-Site Consultation Agreements (29 CFR Part 1908), OMB Control Number 1218-0110, paperwork package to include the approved Process Safety Management On-Site Consultation Agreements (29 CFR 1908), OMB Control Number 1218-0281.

Federal Register Notices

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

Authorizing Statutes

29 USC 670
View Law
29 USC 656
View Law

Presidential Action:

-

Title:

[NCIPC] Comprehensive Evaluation of the Implementation and Uptake of the CDC Clinical Practice Guideline for Prescribing Opioids for Pain

Reference Number:

202412-0920-006

Omb Control Number:

0920-1459

Agency:

HHS/CDC

Received:

2025-01-06

Concluded:

2025-06-09

Action:

Approved with change

Status:

Active

Request Type:

New collection (Request for a new OMB Control Number)
[NCIPC] Comprehensive Evaluation of the Implementation and Uptake of the CDC Clinical Practice Guideline for Prescribing Opioids for Pain

Key Information

Abstract

Data collection is designed to conduct a comprehensive evaluation of the dissemination, implementation, and outcomes of the CDC Clinical Practice Guideline for Prescribing Opioids for Pain – United States, 2022 (2022 CDC Clinical Practice Guideline). Resulting data will be used for purposes of evaluation and to ensure that Americans have access to safer, effective ways of managing their pain.

Federal Register Notices

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

Authorizing Statutes

42 USC 241
View Law

Presidential Action:

-
Subscribe