Information Collection Request (ICR) Tracker
ICR Definition
An Information Collection Request (ICR) is a federal agency’s request for approval from the Office of Management and Budget (OMB) to collect information from the public.
Under the Paperwork Reduction Act (PRA), agencies must justify why the information is needed and how it will be used.
Federal agencies are required to submit an ICR whenever they create, renew, modify, or discontinue an information collection. Each ICR includes a description of the collection,
supporting materials and documentation (such as forms, surveys, or scripts), and proof that the agency has met the requirements of the PRA.
The ICR is submitted to the The Office of Information and Regulatory Affairs (OIRA) within OMB for review and approval. OIRA grants approval for a maximum of three years, after
which the collection must be renewed through a new ICR submission.
ICRs are publicly available on RegInfo.gov, and additional guidance can be found in the FAQs.
ICR Explorer
Showing 20 of 11245 results
Reference Number | Title | Agency | Status | Request Type | ||||||||||||||||
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202504-0920-028 | [NCEZID] Emerging Infections Program | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[NCEZID] Emerging Infections Program
Key Information
Federal Register Notices
Authorizing Statutes42 USC 301 (View Law) AbstractThe Emerging Infections Programs (EIP) is to 1) detect and monitor emerging pathogens, the diseases they cause, and the factors influencing their emergence, and respond to problems as they are identified, 2) integrate laboratory science and epidemiology to optimize public health practice, 3) strengthen infrastructure to support surveillance and research and to implement prevention and control programs, and to 4) ensure implementation of prevention strategies and communication of public health information about emerging diseases. Surveillance efforts of the core EIP activities generate reliable estimates of the incidence of certain infections and provide the foundation for a variety of epidemiologic studies. This Non-Substantive Change Request is submitted to make modifications to 13 data collection forms in the 0920-0978 package for compliance with EO 14168. There is no anticipated change to the approved burden hours. |
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202505-0920-003 | [OADPS] The Performance Measures Project: Improving Performance Measurement and Monitoring by CDC Programs | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[OADPS] The Performance Measures Project: Improving Performance Measurement and Monitoring by CDC Programs
Key Information
Federal Register Notices
Authorizing Statutes42 USC 45 CFR 75.342 (View Law) AbstractThe purpose of this Generic Data Collection is to: 1) help CDC programs and their recipients develop strong performance measurement systems and practices; 2) define and operationalize priority performance measures; and 3) establish common data collection and reporting expectations. Data will enable the accurate, reliable, uniform and timely submission of recipients' progress. This Non-Substantive Change Request is submitted to make modification to the existing/approved GenIC - CDC-RFA-PS-24-0003 Support and Scale-Up of HIV Prevention Services in Sexual Health Clinics (or SHIPS). There is no change to the approved number of burden hours. |
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202504-0920-021 | CDC and ATSDR Health Message Testing System | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
CDC and ATSDR Health Message Testing System
Key Information
Federal Register Notices
Authorizing Statutes42 USC 241 (View Law) AbstractCDC must communicate about hazards, outbreaks and other emergencies that present an urgent health threat to the public. Untested messages can waste communication resources and opportunities because the messages can be perceived as unclear or irrelevant. OADC-CDC requests a reinstatement without change for the generic clearance for an expedited review of items to be used in health message testing to ensure the public will understand health messages and take recommended action. |
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202504-0920-025 | [PHIC] Data Collection for CDC Fellowship Programs | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[PHIC] Data Collection for CDC Fellowship Programs
Key Information
Federal Register Notices
Authorizing Statutes42 USC 241 (View Law) AbstractThe intended use of data collected is to inform the planning, implementation, and continuous quality improvement of CDC Fellowship Programs. Data collection methods include focus groups, interviews, and surveys, using both purposive and probabilistic samples. Respondent populations include potential applicants, fellows, alumni, supervisors, mentors, and employers of alumni. Data will be analyzed relative to the data collection methods and purpose. The Change Request contains minor changes and adheres to recent executive orders. |
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202503-0920-027 | [NCHHSTP] Medical Monitoring Project | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[NCHHSTP] Medical Monitoring Project
Key Information
Federal Register Notices
Authorizing Statutes42 USC 301 (View Law) AbstractThe Medical Monitoring Project (MMP) was designed to address the need for a national behavioral and clinical surveillance system for HIV-infected persons, as articulated in CDC's HIV Prevention Strategic Plan. It is a supplemental surveillance project designed to describe the health-related behaviors, experiences and needs of adults diagnosed with HIV in the United States. It's intended use is to guide national and local HIV-related service organization and delivery and to monitor receipt of HIV treatment and prevention services and clinical outcomes. The changes proposed in this revision update the data collection system to meet prevailing information needs and enhance the value of MMP data, while remaining concordant with the project’s purpose. The burden is the same as the burden shown in the current inventory. |
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202502-1293-001 | Eligibility Data Form: Uniformed Services Employment and Reemployment Rights Act and Veterans' Preference | DOL/ASVET | Active | No material or nonsubstantive change to a currently approved collection
Eligibility Data Form: Uniformed Services Employment and Reemployment Rights Act and Veterans' Preference
Key Information
Federal Register Notices
Authorizing StatutesAbstractTitle 38 U.S.C. Section 4322 of USERRA authorizes the Secretary of Labor (through the Veterans' Employment and Training Service) to investigate claims by individuals who believe their USERRA rights have been violated. The information is used to determine eligibility of veterans complaints to reemployment rights they are seeking as well as to state alleged violations by employers of the pertinent statutes and request assistance in obtaining appropriate reemployment benefits. The Veterans Employment Opportunities Act (VEOA) of 1998, P.L. 105-339, 112 Stat. 3182, contained in Title 5 U.S.C. § 3330a-3330(b), provides assistance to preference eligible individuals who believe their rights under the veterans' preference (VP) laws and the Veterans Benefit Improvement Act of 2008 (Public Law No: 110-389) have been violated. Section 3 of the VEOA provides the Secretary of Labor similar authority to investigate complaints brought by preference eligibles. The collection instrument completed by claimants contains the information required and needed for the Department to determine initial eligibility of the claimant. |
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202401-1018-002 | Administrative Procedures for U.S. Fish and Wildlife Service Financial Assistance Programs | DOI/FWS | Historical Inactive | Revision of a currently approved collection
Administrative Procedures for U.S. Fish and Wildlife Service Financial Assistance Programs
Key Information
Federal Register Notices
Authorizing Statutes16 USC 777 et seq. (View Law) 16 USC 669 et seq. (View Law) AbstractThe Service issues financial assistance through grants and cooperative agreement awards to commercial organizations, foreign entities, Indian tribal governments, individuals, institutions of higher education, non-profit organizations, and state and local governments under the bureau's Assistance Listing (CFDA) programs. The types of assistance provided under Service financial assistance programs include: • Mandatory Formula Grants • Discretionary Project Grants • Discretionary Cooperative Agreements • Use of Property, Facilities, and Equipment Authorities and implementing regulations establish financial assistance program purposes and may specify funding instrument(s), selection criteria, and eligible and ineligible recipients and activities. For competitive programs, the authorities or implementing regulations may establish preferences or ranking factors for the selection of projects. These legal requirements make it essential for an awarding agency to have certain information so that it funds only eligible projects, and, in the case of competitive programs, to select those projects that will result in the greatest return on the Federal investment. |
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202504-0920-007 | [NCHHSTP] National HIV Behavioral Surveillance System | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[NCHHSTP] National HIV Behavioral Surveillance System
Key Information
Federal Register Notices
Authorizing Statutes42 USC 306 (View Law) 42 USC 301 (View Law) AbstractThe National HIV Behavioral Surveillance system (NHBS) is a supplemental surveillance project designed to describe the HIV prevalence and behaviors related to HIV acquisition and prevention among the three populations at highest risk for HIV in the United States: men who have sex with men, persons who inject drugs, and heterosexually active persons at increased risk for HIV infection. For this Revision, interview data collection instruments were revised and the number of health departments participating in the NHBS System will decrease, in addition to other minor changes. |
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202503-0920-004 | [NCEH] Aerosols from cyanobacterial blooms: exposures and health effects in a highly exposed population | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[NCEH] Aerosols from cyanobacterial blooms: exposures and health effects in a highly exposed population
Key Information
Federal Register Notices
Authorizing Statutes42 USC 241 (View Law) AbstractHuman exposures to cyanobacterial toxins have been reported to produce a variety of health effects, including respiratory irritation and liver and kidney damage. The goals of this study are: 1). To assess exposures and health symptoms in people who are exposed to aerosols generated during cyanobacterial harmful algal blooms (CyanoHABs) while living near or working on Lake Okeechobee, Florida and connecting rivers and estuaries and 2). to investigate the relationships. This Non-Substantive Change Request is submitted to expand the potential exposures to HAB aerosols where HABS include marine microalgae; marine macroalgae, such as seaweeds; and cyanobacteria. There is no change to the burden or potential respondents. |
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202504-0920-014 | [NCCDPHP] Pregnancy Risk Assessment Monitoring System (PRAMS) | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[NCCDPHP] Pregnancy Risk Assessment Monitoring System (PRAMS)
Key Information
Federal Register Notices
Authorizing StatutesAbstractWe request a non-substantive change to OMB control number 0920-1273 to 1) remove the current response threshold requirement so all jurisdiction data are available for release to internal and external researchers and 2) change release of PRAMS multi-jurisdiction data from previously documented proposal process to the PRAMS Automated Research File (ARF) process. |
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202501-1240-003 | Uniform Billing Form | DOL/OWCP | Active | Extension without change of a currently approved collection
Uniform Billing Form
Key Information
Federal Register Notices
Authorizing StatutesAbstractOWCP requires institutional medical providers who provide services to beneficiaries covered under the Federal Employees’ Compensation Act (FECA), 5 U.S.C. 8101, the Black Lung Benefits Act (BLBA), 30 U.S.C. 901, and the Energy Employees Occupational Illness Compensation Program Act of 2000 (EEOICPA), 42 U.S.C. 7384, to bill using a form based on the industry standard form approved by the American Hospital Association, the UB-04. Form OWCP-04 identifies the beneficiary, the type of services provided, the conditions being treated and billed amounts. This information is required by OWCP to enable it to pay providers for covered services. |
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202505-0920-001 | [PHIC] The Division of Workforce Development (DWD) Fellowship Alumni Assessment | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[PHIC] The Division of Workforce Development (DWD) Fellowship Alumni Assessment
Key Information
Federal Register Notices
Authorizing Statutes42 USC 241 (View Law) AbstractThis information collection request (ICR) is to gain three-year approval to follow alumni career progression following participation in the Public Health Associate Program (PHAP). The subpopulations to be studied are the PHAP Host Site Supervisors and PHAP Alumni. Information will be collected through online surveys. Findings will be used to assess the quality and value of the PHAP. This change request implements changes to adhere to recent executive orders. |
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202503-0938-001 | Medicare Transaction Facilitator for 2026 and 2027 under Sections 11001 and 11002 of the Inflation Reduction Act (IRA) (CMS-10912) | HHS/CMS | Active | New collection (Request for a new OMB Control Number)
Medicare Transaction Facilitator for 2026 and 2027 under Sections 11001 and 11002 of the Inflation Reduction Act (IRA) (CMS-10912)
Key Information
Federal Register Notices
Authorizing StatutesPub.L. 117 - 169 11001 and 11002 (View Law) AbstractUnder the authority in sections 11001 and 11002 of the Inflation Reduction Act of 2022 (P.L. 117-169), the Centers for Medicare & Medicaid Services (CMS) is implementing the Medicare Drug Price Negotiation Program (“the Negotiation Program”), codified in sections 1191 through 1198 of the Social Security Act (“the Act”). The Act establishes the Negotiation Program to negotiate a maximum fair price (“MFP”), defined at section 1191(c)(3) of the Act, for certain high expenditure, single source drugs covered under Medicare Part B and Part D (“selected drugs”). In accordance with section 1193(a) of the Act, any Primary Manufacturer of a selected drug that continues to participate in the Negotiation Program and reaches agreement upon an MFP must provide access to the MFP to MFP-eligible individuals, defined in section 1191(c)(2)(A) of the Act, and to pharmacies, mail order services, other dispensing entities, providers and suppliers with respect to such MFP-eligible individuals who are dispensed that selected drug during a price applicability period. The purpose of this information collection request (ICR) is for CMS to collect information from manufacturers of drugs covered under Part D selected for negotiation under the Inflation Reduction Act for the initial price applicability years 2026 and 2027 and the dispensing entities that dispense the selected drugs to MFP-eligible individuals. To facilitate the effectuation of the MFP, CMS will engage a Medicare Transaction Facilitator (“MTF”). The MTF system will be comprised of two modules: the MTF Data Module (MTF DM), and the MTF Payment Module (MTF PM). Primary Manufacturers participating in the Negotiation Program are required to participate in the MTF DM. |
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202504-0920-030 | [NCCHPHP] Comprehensive Evaluations of the WISEWOMAN Programs, The National Cardiovascular Health Program, The Innovative Cardiovascular Health Program | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[NCCHPHP] Comprehensive Evaluations of the WISEWOMAN Programs, The National Cardiovascular Health Program, The Innovative Cardiovascular Health Program
Key Information
Federal Register Notices
Authorizing Statutes42 USC 247b (View Law) 42 USC Title IV, Sec. 4002, 300u-11 (View Law) 42 USC Title XV, Sec. 1509 (View Law) 42 USC Sec. 1502, 3001 (View Law) Pub.L. 117 - 328 136 STAT. 4459 (View Law) AbstractThe purpose of the project is to conduct a comprehensive implementation and outcome evaluation to assess the unique contributions of The National Cardiovascular Health Program (The National CVH Program), The Innovative Cardiovascular Health Program (The Innovative CVH Program), and Well-Integrated Screening and Evaluation of Women Across the Nation (WISEWOMAN) cooperative agreements to identify promising cardiovascular disease (CVD) prevention and management practices that can be scaled and replicated, advance health equity, and the transformation of health systems for improved CVD prevention and management. The programs work together to create efficiencies and improve outcomes in jurisdictions that receive funding for two or more of the cooperative agreements. This Evaluation aims to assess implementation, assess the extent to which short-term, intermediate, and long-term outcomes have been met, and estimate the costs involved in program implementation. This Non-Substantive Change Request is submitted to revise questions to align with recent executive orders, EO 14168 and EO 14151. There is no change anticipated to the currently approved burden hours. |
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202504-0524-001 | Veterinary Medicine Loan Repayment Program (VMLRP) | USDA/NIFA | Active | No material or nonsubstantive change to a currently approved collection
Veterinary Medicine Loan Repayment Program (VMLRP)
Key Information
Federal Register Notices
Authorizing Statutes7 USC 3151A (View Law) AbstractThis information collection adds new reporting and record keeping requirements, feedback, surveys and a post-contract survey. |
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202504-0579-004 | Volunteer Service Agreements and Volunteer Service Time and Attendance Record | USDA/APHIS | Active | No material or nonsubstantive change to a currently approved collection
Volunteer Service Agreements and Volunteer Service Time and Attendance Record
Key Information
Federal Register Notices
Authorizing Statutes7 USC 2272 (View Law) AbstractThe purpose of the collection is to collect information necessary to establish guidelines for acceptance of volunteer services, and to make a determination of individuals ' eligibility and suitability to serve as volunteer in Marketing and Regulatory Programs. |
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202502-0584-001 | 2027 Farm to School Census (Renewal) | USDA/FNS | Active | Revision of a currently approved collection
2027 Farm to School Census (Renewal)
Key Information
Federal Register Notices
Authorizing Statutes42 USC 1769 (View Law) Pub.L. 111 - 296 305 (View Law) AbstractThis information collection request is for a revision and extension for three years to the currently approved Farm to School Census and Comprehensive Review (OMB Number 0584-0646, expiration date 5/31/25). The intended purpose of this information collection is to administer the 2027 Farm to School Census. |
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202504-7100-001 | Payments System Surveys | FRS | Active | No material or nonsubstantive change to a currently approved collection
Payments System Surveys
Key Information
Federal Register Notices
Authorizing Statutes12 USC 342 (View Law) 12 USC 411 (View Law) 12 USC 412 (View Law) 12 USC 413 (View Law) 12 USC 414 (View Law) 12 USC 415 (View Law) 12 USC 416 (View Law) 12 USC 417 (View Law) 12 USC 420 (View Law) 12 USC 422 (View Law) 12 USC 248(d) (View Law) 12 USC 248a (View Law) AbstractThe Payment Systems Surveys are used to obtain information specifically tailored to the Federal Reserve’s operational and fiscal agency responsibilities. The Payment Systems Surveys family of surveys currently comprises of the following: • Ad Hoc Payments Systems Survey (FR 3054a), • Currency Quality Sampling Survey (FR 3054b), • Currency Quality Survey (FR 3054c), • Currency Functionality and Perception Survey (FR 3054d), and • Currency Education Usability Survey (FR 3045e). |
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202504-0920-006 | [NCCDPHP] 2025 and 2027 NATIONAL YOUTH RISK BEHAVIOR SURVEY | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[NCCDPHP] 2025 and 2027 NATIONAL YOUTH RISK BEHAVIOR SURVEY
Key Information
Federal Register Notices
Authorizing Statutes42 USC 241 (View Law) AbstractThe school-based National Youth Risk Behavior Survey (YRBS) is a biennial survey of high school students that assesses the priority health-risk behaviors in adolescents related to the major preventable causes of mortality, morbidity, and social problems among both youth and adults in the United States. The YRBS is conducted by the Centers for Disease Control and Prevention (CDC), that assesses priority health-risk behaviors related to the major preventable causes of mortality, morbidity, and social problems among both youth and adults in the United States. Minor changes incorporated into this reinstatement request include: an updated title for the information collection to accurately reflect the years in which the survey will be conducted, a slightly modified questionnaire, and the addition of a smaller study designed to assess the validity of new questions on fruit, vegetable, and energy drink intake that are being considered for inclusion on the 2027 YRBS questionnaire. |
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202504-0920-005 | [NCEZID] CryptoNet Case Report Form | HHS/CDC | Active | No material or nonsubstantive change to a currently approved collection
[NCEZID] CryptoNet Case Report Form
Key Information
Federal Register Notices
Authorizing Statutes42 USC 241 (View Law) AbstractThe goal of the CryptoNet Case Report Form (CRF) is to define a set of data elements that can be used to identify exposure trends in outbreak- and non-outbreak-associated Cryptosporidium cases, to generate hypotheses about the source(s) of infection in clusters or outbreaks, and to identify strategies to prevent and control cases, clusters, or outbreaks. This Revision includes race/ethnicity question modification and updating some laboratory test options. Non-Substantive Change Request is submitted to modify single question for compliance with EO 14168. |
Why They Are Important
ICRs play a vital role in ensuring transparency and accountability in federal data collection. When federal agencies collect information from 10 or more "persons" (which includes individuals,
businesses, and state, local, and tribal governments), they must submit an ICR to ensure that it fulfills their statutory missions, avoids unnecessary or duplicative requests, and
minimizes burden on the American public. Additionally, Federal Register Notices (FRNs) and the opportunity for public comments provide a formal way for the public to be informed of
proposed ICRs and participate in the process.
ICRs also serve as a key resource for tracking changes to federal data collections. The availability of detailed documentation, such as data collection instruments and methodologies,
allows the general public to identify revisions in a timely manner. These may include revisions prompted by Executive Orders or statistical policies like
OMB's Statistical Policy Directive No. 15 (SPD 15), which are often submitted as "nonsubstantive" or "nonmaterial" changes to a
currently approved collection.[1] Furthermore, ICRs can help determine if a data collection has expired without renewal or has been intentionally
discontinued. By reviewing ICRs, the public can better understand what data is being collected, how it evolves over time, and whether data collections have become inactive–often in response
to shifting priorities and updated standards.
How To Use The Tool
The ICR tracking tool offers a user-friendly view of ICRs that have been recently submitted, reviewed, or are nearing expiration. By aggregating key data from individual ICRs,
the tool allows users to view the current status of each request, including submission, conclusion, and expiration dates, details on whether any changes were made, authorizing statutes,
and more. Users can search for specific information and filter results based on various criteria. If seeking additional information, various text fields are hyperlinked to the full ICR
on RegInfo.gov and associated resources. The tool is updated on a daily basis to reflect the most current information available.
Column descriptions are available below the table.
Column Name
Definition
Categories Include
ICRReferenceNumber
The ICR Reference Number uniquely identifies each ICR review. This number is assigned by the OIRA system when the ICR is created.
ICR Reference Numbers are formatted YYYYMM-NNNN-XXX where YYYYMM is the month of origin, NNNN is the agency/subagency code, and XXX is a 3 digit sequential number assigned per creation per month.
N/A
ICRTitle
The title of the information collection. If the submission is a revision to a currently approved collection, the title is the name of the overall collection rather than the name of the change taking place.
N/A
DateReceived
The date OIRA received the ICR submission from the agency.
N/A
OMBControl
OIRA assigns an OMB Control Number to an Information Collection Request (ICR) upon its first arrival. The same OMB Control Number is used for each review of the ICR.
OMB Control Numbers are formatted NNNN-XXXX, where the NNNN is the agency/subagency code, and the XXXX is a sequential number uniquely identifying the Collection within the agency/subagency’s ICRs.
N/A
DateReceived
The date OIRA received the ICR submission from the agency.
N/A
PreviousICRReferenceNumber
The reference number of the ICR that immediately preceded the current one.
N/A
AgencySubagency
The federal agency and specific subagency, if applicable, that submitted the ICR.
N/A
Abstract
A brief statement describing the need for the collection of information and how it will be used.
N/A
RequestType
Describes the purpose of the agency's submission.
- "Extension without change of a currently approved collection"
- "Existing collection in use without an OMB Control Number"
- "Reinstatement with change of a previously approved collection"
- "New collection (Request for a new OMB Control Number)"
- "No material or nonsubstantive change to a currently approved collection"
- "Revision of a currently approved collection"
- "Reinstatement without change of a previously approved collection"
- "RCF Recertification"
- "RCF No Material or nonsubstantive change to a currently approved collection"
- "RCF New"
TypeOfReviewRequest
Indicates the specific type of action being requested for review.
- "Regular"
- "Emergency"
- "Delegated"
Status
Indicates the current stage of the ICR in OIRA's review process.
- "Received in OIRA" for ICRs currently under review by OIRA
- "Active" for ICRs that are currently approved for use by agencies
- "Historical Active" for previous reviews of ICRs that are currently in the active inventory
- "Historical Inactive" for previous reviews of ICRs that are not currently in the active inventory
- "PreApproved" for ICRs that will become active once the Final Rule of their associated rulemaking has been published
ConcludedDate
The date OIRA completed its review of the ICR.
N/A
ConclusionAction
OIRA's final decision about the ICR.
- “Comment filed on Interim Final Rule”
- “Comment filed on Interim Final Rule and continue”
- “Disapproved”
- “Approved without change”
- “Approved with change”
- “Comment filed on proposed rule”
- “Preapproved”
- “Withdrawn”
- “Withdrawn and continue”
- “Not subject to PRA”
- “Not subject to PRA and continue”
- “Improperly submitted”
- “Improperly submitted and continue”
- “Delegated”
- “Comment filed on proposed rule and continue”
- “Disapproved and continue”
- “Returned - Improperly Submitted”
- “Returned to Agency for Reconsideration”
- “Returned - Outside Generic Clearance”
- “Approved”
CurrentExpirationDate
The date the ICR is set to expire unless it is renewed.
N/A
AuthorizingStatues
Names of federal laws that authorize the agency to collect the information.
N/A
AuthorizingStatuesDetails
Additional details about the legal authority for the information collection, including a URL linking to the full text.
N/A
CitationsForNewStatutoryRequirements
Legal citations that have introduced new or modified statutory requirements since the last ICR submission.
N/A
FederalRegisterNotices
Lists citations of 60-day and 30-day notices published in the Federal Register.
N/A
PublicCommentsReceived
Indicates whether any public comments were received during the Federal Register notice period.
N/A
InformationCollections
Lists the individual information collections associated with the ICR. Each collection includes metadata such as the title, a URL to the collection, the form number (if applicable), and a URL to the form.
N/A
RequestType Filters
1. Select "New collection (Request for an OMB Control Number)" for collections that had not previously been used or sponsored by the agency.
2. Select "Extension without change or a currently approved collection" for collections where the agency wished only to extend the approval of an active collection past its current expiration date without making any material change in the collection instrument, instructions, frequency of collection, or the use to which the information is to be put.
3. Select "Revision of a currently approved collection" for collections where the agency request included a material change to the collection instrument, instructions, its frequency of collection, or the use to which the information is to be put.
4. Select "Reinstatement without change of a previously approved collection" for collections which previously had OMB approval, but the approval had expired or was discontinued before this submission was made, and there is no change to the collection.
5. Select "Reinstatement with change of a previously approved collection" for collections which previously had OMB approval, but the approval has expired or was discontinued before this submission was made, and there is some change to the collection.
6. Select "Existing collection in use without OMB control number" when the collection is currently in use but does not have an OMB control number.
7. Select "No material or nonsubstantive change to a currently approved collection" for collections which introduce minor changes to the ICR, but do not extend the expiration date of the collection.
8. Select "RCF No material or nonsubstantive change to a currently approved collection" for RCF collections that introduce changes to the usage of an active RCF.
9. Select "RCF New" for RCF collections that are the initial usage of the Common Form Host ICR by the using agency.
10. Select "RCF Recertification" for RCF collections that had been recertified due to changes in its related Common Form Host ICR.
[1] "Nonsubstantive" and "nonmaterial" changes introduce minor modifications to the ICR but do not extend the collection's expiration date or require a public comment period.