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 429 results
Reference Number | Title | Agency | Received | Status | Request Type | ||||||||||||||||||||
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202502-0970-050 | Personal Responsibility Education Program (PREP) Performance Measures | HHS/ACF | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
Personal Responsibility Education Program (PREP) Performance Measures
Key Information
Federal Register Notices
Authorizing StatutesPub.L. 114 - 10 215 (View Law) 31 USC 1101 (View Law) AbstractThe consequences of adolescent sexual activity remain a critical social and economic issue in the United States, shaping the lives of thousands of teens and their families every year. Despite declining births to teen mothers over the past 25 years, the teen birthrate in the United States remains higher than that in other industrialized countries and varies widely across geographic regions and racial/ethnic groups (Martin et al. 2017). Further, adolescents and young adults account for half of all new sexually transmitted infection (STI) cases each year (Centers for Disease Control and Prevention 2022). Sexual activity in youth is also related to engaging in other risky behaviors such as alcohol and substance use. In March 2010, Congress authorized the Personal Responsibility Education Program (PREP) as part of the Patient Protection and Affordable Care Act (ACA). PREP provides grants to states, tribes and tribal communities, and community organizations to support evidence-based programs to reduce teen pregnancy and STIs. The programs are required to provide education on both abstinence and contraceptive use. The programs also offer information on adulthood preparation subjects such as healthy relationships, adolescent development, financial literacy, parent–child communication, education and employment skills, and healthy life skills. Grantees are encouraged to target their programming to high-risk populations—for example, youth in foster care, homeless youth, youth with HIV/AIDS, pregnant youth who are under age 21, mothers who are under age 21, and youth residing in geographic areas with high teen birth rates. The Government Performance and Results Act (GPRA) Modernization Act of 2010 (Public Law 111-352) requires federal agencies to report annually on measures of program performance. It is essential that PREP grantees report the performance data described in this information collection request to enable the Administration for Children and Families to carry out its reporting requirements to Congress and the Office of Management and Budget. This request seeks to (1) to extend the previously approved data collection of the performance measures from PREP grantees with proposed revisions. Specifically, ACF is requesting approval to eliminate the requirement for grantees to aggregate participant survey data to the program level for submission starting with the 2023-2024 data. Updates made to program-level data collection forms (Instruments 3b and 4b) reflect this request. Grantees will continue to use the currently approved data collection forms (Instruments 3a and 4a) for submission of 2022-2023 data. Additionally, we are requesting a study name change from Personal Responsibility Education Program (PREP) Performance Measures and Adulthood Preparation Subjects Study (PREP PMAPS) to Personal Responsibility Education Program (PREP) Performance Measures, as the data collection for the Adulthood Preparation Subjects Study is complete. The following ICR has been updated with non substantive changes in response to the Defending Women from Gender Ideology Extremism and Restoring Biological Truth to the Federal Government Executive Order (Defending Women EO) and recent Presidential Actions related to diversity, equity, and inclusion (DEI), such as those covered under the EO Initial Recissions of Harmful Executive Orders and Actions. |
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202503-0906-002 | Voluntary Partner Surveys to Implement Executive Order 12862 in the Health Resources and Services Administration | HHS/HRSA | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
Voluntary Partner Surveys to Implement Executive Order 12862 in the Health Resources and Services Administration
Key Information
Federal Register Notices
AbstractThis generic project clearance allows HRSA to conduct voluntary customer satisfaction surveys of its partners to assess strengths and weaknesses in program services and products. Examples of such surveys include satisfaction with technical assistance provided to grantees, in class evaluations of training sessions, and satisfaction with information services. |
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202503-0920-024 | [NCCDPHP] CDC Diabetes Prevention Recognition Program (DPRP) | HHS/CDC | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
[NCCDPHP] CDC Diabetes Prevention Recognition Program (DPRP)
Key Information
Federal Register Notices
Authorizing Statutes42 USC 1302, 1395hh (View Law) 42 USC 301 (View Law) AbstractCDC's Division of Diabetes Translation's (DDT) National Diabetes Prevention Program Diabetes Prevention Recognition Program (DPRP) Revision of the DPRP Standards and Operating Procedures. Research studies have shown that a structured lifestyle intervention leading to modest weight loss and increased physical activity can prevent or delay type 2 diabetes. To this end, DDT established and administers the DPRP. Organizations participate on a voluntary basis. There are a few revisions that are being requested, and they are listed in the SSA and a stand alone document. |
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202503-0920-007 | [NCEH] Environmental Public Health Tracking Network (Tracking Network) | HHS/CDC | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
[NCEH] Environmental Public Health Tracking Network (Tracking Network)
Key Information
Federal Register Notices
Authorizing Statutes42 USC 247 (View Law) AbstractCDC's Tracking Program collects, integrates, analyzes, and disseminates data on health, exposure, environmental hazards, and populations in order to drive public health actions that mitigate or prevent the effects of environmental factors on the health of communities. Respondents include 26 funded grantees and unfunded state and local health departments (SLHD). These data are used to describe trends, identify populations at risk, generate hypotheses, and inform public health actions for SLHD. Additional program information collected quarterly or annually are used to evaluate and assess program performance is collected using 6 forms. This change request is to adhere to current executive orders. |
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202503-0920-011 | [NIOSH] Reducing Fatigue Among Taxi/Rideshare Drivers | HHS/CDC | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
[NIOSH] Reducing Fatigue Among Taxi/Rideshare Drivers
Key Information
Federal Register Notices
Authorizing Statutes29 USC 657(g) (View Law) AbstractThe goal of this study is to evaluate an online, interactive training on fatigue management tailored to taxi drivers and other for-hire rideshare drivers. The proposed study is a longitudinal, randomized design comparing two interventions and a control over 5 study periods. One group of 60 drivers will receive both interventions: fatigue training and daily feedback on estimated fatigue score. A second group of 60 drivers will receive only the fatigue training. A third group of 60 drivers will receive neither intervention. All participating drivers will take a self-administered questionnaire, wear a wrist actigraph to measure sleep quality, complete a sleep and activities diary, and take a sleep health and driving knowledge assessment. Drivers taking the training will be asked to complete an evaluation. Findings will be used to improve the training program for potential future dissemination. This change request updates documents to follow executive orders. |
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202503-0920-009 | The National Violent Death Reporting System (NVDRS) | HHS/CDC | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
The National Violent Death Reporting System (NVDRS)
Key Information
Federal Register Notices
Authorizing Statutes42 USC 301 (View Law) AbstractThe National Violent Death Reporting System (NVDRS) collects information for surveillance to monitor the occurrence of violent deaths in the U.S. at the national, state, and local levels. Data is used to understand magnitude, trends, and characteristics of violent death and what factors protect people or put them at risk for experiencing violence. This revision includes 1) updates to the web-based system to improve performance, functionality, and accessibility, 2) new variables, 3) addition of a School Associated Violent Death (SAVD) module to prepare for discontinuation of OMB No. 0920-0604, and 4) addition of a Public Safety Officer suicide module. |
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202503-0920-034 | [NCHHSTP] National HIV Behavioral Surveillance: Brief HIV Bio-behavioral Assessment (NHBS-BHBA) | HHS/CDC | 2025-03-28 | Historical Inactive | No material or nonsubstantive change to a currently approved collection
[NCHHSTP] National HIV Behavioral Surveillance: Brief HIV Bio-behavioral Assessment (NHBS-BHBA)
Key Information
Federal Register Notices
Authorizing Statutes42 USC 241 (View Law) AbstractThe primary objective of NHBS-BHBA is to conduct mixed-methods behavioral surveillance among populations at high risk for HIV in selected geographic areas of interest to assess: 1) risk behaviors and social determinants of health for HIV infection, 2) HIV testing behaviors and treatment, 3) HIV seroprevalence and incidence, and 4) exposure to, use of, and impact of HIV prevention services. Through this project, funded state health departments for NHBS-BHBA will work with local entities to collect surveillance data to understand HIV risk, especially in areas or populations with limited information. Non-Substantive Change Request submitted to modify package documents for compliance with recently issued EOs. There is no change anticipated to the burden hours. |
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202503-0970-002 | ACF’s Generic Clearance for Reviewer Recruitment Forms | HHS/ACF | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
ACF’s Generic Clearance for Reviewer Recruitment Forms
Key Information
Federal Register Notices
AbstractThis request by the Administration for Children and Families (ACF) is to extend approval of the generic clearance for Reviewer Recruitment Forms with no changes (note that burden estimates have been updated to reflect ongoing collections and estimated future burden, but the purpose and use of this generic have not changed). ACF may recruit reviewers for a variety of different activities and each program office within ACF has a slightly different needs for information about reviewer applicants for different activities. This overarching generic clearance allows ACF to request slightly different information from potential reviewers, yet the individual forms serve the same general function. The abbreviated clearance process of the generic clearance allows program offices to gather a suitable pool of candidates within the varied time periods available for reviewer recruitment. The forms submitted under this umbrella generic are and will be voluntary, low-burden and uncontroversial. Information will be collected electronically unless specified otherwise in an individual generic information collection (GenIC) request. |
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202503-0970-006 | Generic for ACF Program Monitoring Activities | HHS/ACF | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
Generic for ACF Program Monitoring Activities
Key Information
Federal Register Notices
AbstractThis information collection request (ICR) is for a revision to the umbrella Generic for ACF Program Monitoring Activities. The current expiration date is November 30, 2023. The overall proposed purposes, uses, and scope of the umbrella remain unchanged. The only changes are to the burden estimates, as described in sections A12 and A15. The Generic for ACF Program Monitoring Activities allows Administration for Children and Families (ACF) program offices to collect standardized information from recipients that receive Federal funds to ensure oversight, evaluation, support purposes, and stewardship of Federal funds. The information is necessary to ensure compliance with Federal and programmatic requirements, monitor progress on recipient activities, and determine and respond to recipient needs such as Training and Technical Assistance (T/TA). ACF is primarily a grant-making agency that promotes the economic and social well-being of families, children, individuals and communities with partnerships, funding, guidance, T/TA. ACF program offices have evolving monitoring needs, dependent on both internal and external factors, such as but not limited to: current grantee activities, needs; uses of federal funds; changes to aspects of programs based on statutory authority, federal regulations or policy, and/or Congressional appropriations; availability of program office funds for site visits (v. desk monitoring); matters of importance related to national health and safety needs of the public, or other events that lead to program changes. There are times when standardized collections of information would be helpful for program offices as they monitor recipient activities and needs. This generic clearance allows program offices the flexibility to create tailored information collections based on current circumstances and to receive approval for these in a timely manner. This is important to allow for ACF’s: • monitoring of compliance with federal practice, guidelines and requirements, • quick understanding of and remediation to national, regional, and/or site-specific issues, • provision of support as needed, • accurate assessment of the efficiency and efficacy of recipient activities • documentation of promising practice, innovative services, and program strengths • flexible and responsive oversight of federal funds |
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202503-0920-008 | [NCEZID] Traveler-based Genomic Surveillance | HHS/CDC | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
[NCEZID] Traveler-based Genomic Surveillance
Key Information
Federal Register Notices
Authorizing StatutesAbstractThe goal of the study is to amend one question on our list of potential additional questions to support data collection for a winter 2023/2024 pilot project. There is a continuous need to have no more than four of the additional questions added to the primary instrument at any given time, there is no additional burden to the participant. The responses to these questions will be collected using the same digital questionnaire as the primary instrument. The PRA-approved supporting statement A (SSA) and consent form both indicate the potential for testing for additional pathogens, and the data collected from this additional question is necessary for the interpretation of test results from the pathogens for which are now testing. This change request modifies the collection to adhere to current execute orders. |
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202503-0915-001 | National Healthy Start Evaluation and Quality Assurance | HHS/HSA | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
National Healthy Start Evaluation and Quality Assurance
Key Information
Federal Register Notices
Authorizing StatutesPub.L. 110 - 339 122 (View Law) 42 USC 254c-8 (View Law) AbstractThe goal of this ongoing monitoring and evaluation is to assess Healthy Start (HS) progress towards meeting its performance goals. Results from monitoring and evaluation efforts will provide actionable evidence to support the improvement, sustainability, replication, and dissemination of the program. The information collected will be used to obtain consistent information across all 100 grantees about HS, its participants, and its outcomes. Respondents include pregnant women and women of reproductive age that were served by HS and HS staff. This revision seeks to reduce the burden of data collection on grantees and program participants, as well as to focus the evaluation more clearly on progress towards meeting performance goals regarding program impact. In the process, this will ensure that collected data is meaningful for monitoring and evaluation, and that previously separate data systems can be streamlined, thus improving efficiency. |
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202502-1122-003 | Office on Violence Against Women Grant Program Notice of Funding Opportunity Template | DOJ/OVW | 2025-03-28 | Active | Revision of a currently approved collection
Office on Violence Against Women Grant Program Notice of Funding Opportunity Template
Key Information
Federal Register Notices
Authorizing StatutesPub.L. 106 - 386 DivisionB (View Law) Pub.L. 113 - 4 Violence Against Women (View Law) Pub.L. 133 - 322 TitleIV Violence Against Women (View Law) Pub.L. 109 - 162 Titles I-IX (View Law) Pub.L. 117 - 103 Division W (View Law) AbstractOVW developed a notice of funding opportunity (NOFO) template and an accompanying Application Guide to assist potential grantees in applying for current OVW programs and related funding opportunities. The NOFO template ensures that all applicants to OVW grant programs and related funding opportunities will be asked to provide uniform information in a consistent manner. OVW developed a NOFO template and an accompanying Application Companion Guide to assist potential applicants with applying to OVW grant programs. The NOFO template ensures that all applicants to OVW grant programs will be asked to provide uniform information in a consistent manner. The information addressed in the NOFO template includes: Application for Federal Assistance; Proposal Abstract; Pre-Award Risk Assessment; Summary Data Sheet; Proposal Narrative; Budget Detail Worksheet and Narrative; Indirect Cost Rate Agreement (if applicable); Disclosure of Process Related to Executive Compensation (if applicable); Memorandum of Understanding; Certification Regarding Compliance with Federal Immigration Law (if applicable); Letter of Nonsupplanting; Confidentiality Notice Form; Disclosure of lobbying Activities (if applicable); Summary of Other Federal Funding (if applicable); Delivery of Legal Assistance Certification (if applicable); and other Program-Specific Items. Each NOFO will then be tailored to address the specific OVW grant program so that identification of eligible applicants, availability of funds, award period, award amount, program scope, other program eligibility requirements; out-of -scope activities, and unallowable costs will be consistent with the statutory requirements and funding amounts authorized for each particular grant program or funding opportunity. |
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202502-0970-043 | Culture of Continuous Learning Project: Case Study | HHS/ACF | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
Culture of Continuous Learning Project: Case Study
Key Information
Federal Register Notices
Authorizing StatutesAbstractOn March 17, 2023, we received OMB approval to conduct a descriptive case study for the Culture of Continuous Learning Project: Case Study (OMB #0970-0605). The purpose of this project is to document the factors that contribute to the feasibility of implementing the Breakthrough Series Collaborative (BSC) quality improvement methodology in Head Start and child care centers. The OMB-approved information collection includes: (1) implementation materials (e.g., worksheets); (2) key informant interviews; (3) focus groups with key staff, teachers, and parents; and (4) surveys with administrators, teachers, staff, and parents. The following ICR has been updated with non substantive changes in response to the Defending Women from Gender Ideology Extremism and Restoring Biological Truth to the Federal Government Executive Order (Defending Women EO) and recent Presidential Actions related to diversity, equity, and inclusion (DEI), such as those covered under the EO Initial Recissions of Harmful Executive Orders and Actions. |
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202502-0970-005 | Tribal Maternal, Infant, and Early Childhood Home Visiting Program Data Reports: Demographic and Service Utilization, Grantee Performance Measures and Quarterly Performance Reports | HHS/ACF | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
Tribal Maternal, Infant, and Early Childhood Home Visiting Program Data Reports: Demographic and Service Utilization, Grantee Performance Measures and Quarterly Performance Reports
Key Information
Federal Register Notices
Authorizing StatutesPub.L. 117 - 328 511 (View Law) AbstractSection 511 Title V of the Social Security Act created the Maternal, Infant, and Early Childhood Home Visiting (MIECHV) Program and authorized the Secretary of the Department of Health and Human Services (HHS) to award grants to Indian tribes (or a consortium of Indian tribes), tribal organizations, or urban Indian organizations. The most recent reauthorization of the MIECHV program set aside 6 percent of the total MIECHV program appropriation for grants to tribal entities and indicates that the Tribal MIECHV grants, to the greatest extent practicable, be consistent with the requirements of the MIECHV grants to states and territories and include conducting a needs assessment and establishing benchmarks. The following ICR has been updated with non substantive changes in response to the Defending Women from Gender Ideology Extremism and Restoring Biological Truth to the Federal Government Executive Order (Defending Women EO) and recent Presidential Actions related to diversity, equity, and inclusion (DEI), such as those covered under the EO Initial Recissions of Harmful Executive Orders and Actions. |
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202502-0970-048 | Supporting Youth to be Successful in Life (SYSIL) Study | HHS/ACF | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
Supporting Youth to be Successful in Life (SYSIL) Study
Key Information
Federal Register Notices
Authorizing Statutes42 USC 5106(b)(5) (View Law) Pub.L. 11 - 320 105(b)(5) (View Law) AbstractOMB approved the impact and implementation studies and instruments for the OPRE Study, Supporting Youth to be Successful in Life (SYSIL) on July 27, 2021 (OMB #0970-0574). Baseline data collection with youth for the impact study began in September 2021. Data collection for the 6-month and 12-month follow-up surveys began in April 2022 and October 2022, respectively. The first round of check-in calls began late 2022 and is complete. The second round of check-in calls began February 2024 and is complete. The first round of interviews and focus groups began May 2022 and is complete. The following ICR has been updated with non substantive changes in response to the Defending Women from Gender Ideology Extremism and Restoring Biological Truth to the Federal Government Executive Order (Defending Women EO) and recent Presidential Actions related to diversity, equity, and inclusion (DEI), such as those covered under the EO Initial Recissions of Harmful Executive Orders and Actions. |
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202503-0920-031 | [NCCDPHP] Message Testing for Tobacco Communication Activities | HHS/CDC | 2025-03-28 | Historical Inactive | No material or nonsubstantive change to a currently approved collection
[NCCDPHP] Message Testing for Tobacco Communication Activities
Key Information
Federal Register Notices
Authorizing Statutes42 USC 301 (View Law) Pub.L. 111 - 148 399-V (View Law) AbstractIn 2012, CDC/OSH obtained OMB approval of a generic clearance to support the development of tobacco-related health messages (Message Testing for Tobacco Communication Activities (MTTCA), OMB No. 0920-0910). The MTTCA clearance has been used to obtain OMB approval for a variety of message testing activities. CDC is requesting OMB approval to extend the generic MTTCA clearance for three years. CDC will continue to use the MTTCA clearance to develop and test messages and materials for current and future phases of the ACA-funded media campaign, as well as OSH's ongoing programmatic initiatives including, but not limited to, the Media Campaign Resource Center, reports from the Office of the Surgeon General, and other communication efforts and materials. The MTTCA generic clearance may also be used to facilitate the development of tobacco-related health communications of interest for CDC collaborative efforts with other federal partners including, but not limited to, the Food and Drug Administration, the Substance Abuse and Mental Health Services Administration, the National Institutes of Health, and the National Cancer Institute. The MTTCA clearance is sufficient to test tobacco related messages developed by CDC. No modification is requested for information collection activities or methodology. Non-Subsantive Change Request is submitted to modify questions in previously approved GenIC for compliance with recently issued EOs. There is no change to burden hours. |
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202503-0915-002 | Maternal and Child Health Services Block Grant Application/Annual Report Guidance | HHS/HSA | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
Maternal and Child Health Services Block Grant Application/Annual Report Guidance
Key Information
Federal Register Notices
Authorizing StatutesPub.L. 101 - 239 501 (View Law) AbstractThe Application and Annual Report fulfill the requirements of Section 505 and Section 506, respectively, of the Title V legislation. Consistent with previous editions, the updated Application/Annual Report Guidance is designed to allow states flexibility in meeting the unique needs of their MCH populations while enabling the Maternal and Child Health Bureau (MCHB) to meet the Title V legislative requirements, collect and utilize comparative data for addressing national and state MCH priorities, and demonstrate accountability in the use of the Federal Title V funds. The MCHB, in the Health Resources and Services Administration (HRSA), serves as the Health and Human Services (HHS) Secretary’s delegate to collect this information and to review it prior to the award of approximately $581 million annually in state formula grants under the MCH Block Grant. This is a revision request. |
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202503-0920-005 | [NCBDDD] Population-based Surveillance of Outcomes, Needs, and Well-being of Children and Adolescents with Congenital Heart Defects | HHS/CDC | 2025-03-28 | Historical Inactive | No material or nonsubstantive change to a currently approved collection
[NCBDDD] Population-based Surveillance of Outcomes, Needs, and Well-being of Children and Adolescents with Congenital Heart Defects
Key Information
Federal Register Notices
Authorizing Statutes42 USC 241, 247b-4 and 280g-13 (View Law) AbstractData from U.S. state birth defect surveillance systems, or population-based studies derived from them, will be used to identify a population-based sample of children and adolescents 2 to 17 years of age born with congenital heart defects (CHD). Surveys will be mailed to their caregivers inquiring about the child’s cardiac and other healthcare utilization, barriers to health care, quality of life, social and educational outcomes, and transition of care from childhood to adulthood as well as the needs and experiences of caregivers. Collected information will be used to inform current knowledge, allocate resources, develop services, and, ultimately, improve long-term health of children and adolescents born with CHD. This change request is to update instruments based on current executive orders. |
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202503-0920-018 | [NIOSH] Assessing Fatigue and Fatigue Management in U.S. Onshore Oil and Gas Extraction | HHS/CDC | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
[NIOSH] Assessing Fatigue and Fatigue Management in U.S. Onshore Oil and Gas Extraction
Key Information
Federal Register Notices
Authorizing StatutesPub.L. 91 - 596 29 USC 669 (View Law) AbstractThis information collection request (ICR) facilitates agency initiation and conduct of the investigation of fatigue and fatigue management in land-based Oil and Gas Extraction (OGE) workers in the United States. Collection of information may help a) identify occupational and non-occupational determinants of fatigue in OGE workers; b) identify worker and organizational factors to consider when developing and implementing fatigue management strategies in the OGE industry; and c) describe how fatigue mitigation strategies are currently being used in the onshore OGE industry. |
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202503-0920-021 | [NIOSH] National Firefighter Registry for Cancer | HHS/CDC | 2025-03-28 | Active | No material or nonsubstantive change to a currently approved collection
[NIOSH] National Firefighter Registry for Cancer
Key Information
Federal Register Notices
AbstractThe main goal of the National Firefighter Registry (NFR), according to the Firefighter Cancer Registry Act of 2018, is, “to develop and maintain a voluntary registry of firefighters to collect relevant health and occupational information of such firefighters for purposes of determining cancer incidence.” This Non-Substantive Change Request is submitted for the following reason(s): 1) Modification of R/E question to follow the recently released Statistical Policy Directive 15 (SPD-15) Standard in the NFR Enrollment Questionnaire; 2) Removal of three questions in the Enrollment Questionnaire that are being asked exclusively in the User Profile; and 3) Modification of Sex question to conform to EO 14168. There is no change to the burden hours approved for this data collection. |
ICR Data Dictionary
Field
Description
Example
Reference Number
Unique identifier for an ICR submission, consisting of the year, agency code, and submission number.
202212-1505-001
Title
Name of the information collection.
Annual Survey of Manufactures
Agency
Federal agency and subagency responsible for the information collection.
Department of Commerce/Census Bureau
Status
Current status of the ICR in the review process.
Active, Concluded, Withdrawn
Request Type
Type of request being made (e.g., new collection, extension, revision).
New Collection, Extension, Revision
OMB Control Number
Identifier assigned by OMB to approved information collections.
0607-0449
Abstract
Brief description of the information collection's purpose and use.
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.