{"description":"Documents matching 'currently fall under control associated'","count":10000,"total_pages":50,"next_page_url":"https://www.federalregister.gov/api/v1/documents?conditions%5Bterm%5D=currently+fall+under+control+associated&format=json&page=2","results":[{"title":"Registering NFA Firearms That Fall Out of Government Contract","type":"Proposed Rule","abstract":"The Bureau of Alcohol, Tobacco, Firearms, and Explosives (\"ATF\") proposes amending Department of Justice (\"Department\") regulations implementing a statutory exemption and a statutory authority to grant relief from certain National Firearms Act (\"NFA\") requirements to better distinguish between them. ATF also proposes to amend manufacturer registration requirements to include a provision granting relief to manufacturers from registering firearms they manufacture for the U.S. Government (\"USG\"). In conjunction with this, ATF is proposing a new provision permitting manufacturers to register such firearms \"late\"--after the existing regulatory window for registering manufactured firearms--if they fall out of USG contract.","document_number":"2026-13586","html_url":"https://www.federalregister.gov/documents/2026/07/06/2026-13586/registering-nfa-firearms-that-fall-out-of-government-contract","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-07-06/pdf/2026-13586.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-13586.pdf?1782996321","publication_date":"2026-07-06","agencies":[{"raw_name":"DEPARTMENT OF JUSTICE","name":"Justice Department","id":268,"url":"https://www.federalregister.gov/agencies/justice-department","json_url":"https://www.federalregister.gov/api/v1/agencies/268","parent_id":null,"slug":"justice-department"},{"raw_name":"Bureau of Alcohol, Tobacco, Firearms, and Explosives","name":"Alcohol, Tobacco, Firearms, and Explosives Bureau","id":19,"url":"https://www.federalregister.gov/agencies/alcohol-tobacco-firearms-and-explosives-bureau","json_url":"https://www.federalregister.gov/api/v1/agencies/19","parent_id":268,"slug":"alcohol-tobacco-firearms-and-explosives-bureau"}],"excerpts":"information on <span class=\"match\">current</span> expenses for NFA firearm manufacturers with respect to NFA firearms that <span class=\"match\">fall</span> out of USG contracts: \n 1. Are you <span class=\"match\">currently</span> able to refurnish or resell NFA firearms (other than destructive devices) that <span class=\"match\">fall</span> out of a USG contract? \n 2. How often do you, as an NFA manufacturer, or NFA manufacturers collectively, have such NFA firearms that <span class=\"match\">fall</span> out of a USG contract in a given year? \n 3. How much does it cost to destroy such NFA firearms that <span class=\"match\">fall</span> out of a USG contract? \n 4. How often do you have to destroy NFA firearms that <span class=\"match\">fall</span> out of"},{"title":"Agency Information Collection Activities; USGS Ash Fall Report","type":"Notice","abstract":"In accordance with the Paperwork Reduction Act (PRA) of 1995, the U.S. Geological Survey (USGS) is proposing to renew an information collection.","document_number":"2026-04155","html_url":"https://www.federalregister.gov/documents/2026/03/03/2026-04155/agency-information-collection-activities-usgs-ash-fall-report","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-03-03/pdf/2026-04155.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-04155.pdf?1772459110","publication_date":"2026-03-03","agencies":[{"raw_name":"DEPARTMENT OF THE INTERIOR","name":"Interior Department","id":253,"url":"https://www.federalregister.gov/agencies/interior-department","json_url":"https://www.federalregister.gov/api/v1/agencies/253","parent_id":null,"slug":"interior-department"},{"raw_name":"Geological Survey","name":"Geological Survey","id":212,"url":"https://www.federalregister.gov/agencies/geological-survey","json_url":"https://www.federalregister.gov/api/v1/agencies/212","parent_id":253,"slug":"geological-survey"}],"excerpts":"show ash <span class=\"match\">fall</span> reports in chronological order with key fields including (1) date and time of ash <span class=\"match\">fall</span>, (2) location, (3) positive or negative ash <span class=\"match\">fall</span>, (4) name of observer, and (5) contact. Information is easily viewable internally on the report so that calls for clarification can be made by AVO staff quickly and so that operations room staff can visualize ashfall information quickly. \n Ash <span class=\"match\">fall</span> report data will also be displayed on a dynamic map interface and show positive (yes ash) and negative (no ash) ash <span class=\"match\">fall</span> reports by location. Ash <span class=\"match\">fall</span> reports"},{"title":"Adding Component Definitions Under the Arms Export Control Act","type":"Proposed Rule","abstract":"The Bureau of Alcohol, Tobacco, Firearms, and Explosives (\"ATF\") proposes amending Department of Justice (\"Department\") regulations to include terms that the United States Munitions List uses to describe the composition of defense articles (\"compositional terms\"). Specifically, the proposed rule would amend Department regulations that implement the Arms Export Control Act (\"AECA\") to define the compositional terms \"component,\" \"accessories and attachments,\" and \"part\" for purposes of permanent imports under the AECA.","document_number":"2026-08921","html_url":"https://www.federalregister.gov/documents/2026/05/06/2026-08921/adding-component-definitions-under-the-arms-export-control-act","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-05-06/pdf/2026-08921.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-08921.pdf?1777985129","publication_date":"2026-05-06","agencies":[{"raw_name":"DEPARTMENT OF JUSTICE","name":"Justice Department","id":268,"url":"https://www.federalregister.gov/agencies/justice-department","json_url":"https://www.federalregister.gov/api/v1/agencies/268","parent_id":null,"slug":"justice-department"},{"raw_name":"Bureau of Alcohol, Tobacco, Firearms, and Explosives","name":"Alcohol, Tobacco, Firearms, and Explosives Bureau","id":19,"url":"https://www.federalregister.gov/agencies/alcohol-tobacco-firearms-and-explosives-bureau","json_url":"https://www.federalregister.gov/api/v1/agencies/19","parent_id":268,"slug":"alcohol-tobacco-firearms-and-explosives-bureau"}],"excerpts":"transactions.” 28 CFR 0.130(a)(6)(vi).\n \n \n 3 \n  In Attorney General Order Number 6353-2025, the Attorney General delegated authority to the Director to issue regulations pertaining to matters within ATF's jurisdiction, including <span class=\"match\">under</span> the National Firearms Act, Gun <span class=\"match\">Control</span> Act, and Title XI of the Organized Crime <span class=\"match\">Control</span> Act. ATF's jurisdiction also includes the AECA and the Contraband Cigarette Trafficking Act.\n \n \n \n In carrying out such functions, the Attorney General, and, pursuant to the Attorney General's delegated authority, the Director “shall"},{"title":"Procedures for Chemical Risk Evaluation Under the Toxic Substances Control Act (TSCA)","type":"Proposed Rule","abstract":"The U.S. Environmental Protection Agency (EPA, \"the Agency\") is proposing to amend the procedural framework rule for conducting existing chemical risk evaluations under the Toxic Substances Control Act (TSCA). When conducting an existing chemical risk evaluation under TSCA, EPA must determine whether a chemical substance presents an unreasonable risk of injury to health or the environment, without consideration of costs or non-risk factors, including unreasonable risk to a potentially exposed or susceptible subpopulation identified as relevant to the risk evaluation, under the conditions of use. In this action, EPA proposes to rescind or revise certain 2024 amendments to the procedural framework rule to effectuate the best reading of the statute and ensure that the procedural framework rule does not impede the timely completion of risk evaluations or impair the effective and efficient protection of health and the environment.","document_number":"2025-18431","html_url":"https://www.federalregister.gov/documents/2025/09/23/2025-18431/procedures-for-chemical-risk-evaluation-under-the-toxic-substances-control-act-tsca","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-09-23/pdf/2025-18431.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-18431.pdf?1758545119","publication_date":"2025-09-23","agencies":[{"raw_name":"ENVIRONMENTAL PROTECTION AGENCY","name":"Environmental Protection Agency","id":145,"url":"https://www.federalregister.gov/agencies/environmental-protection-agency","json_url":"https://www.federalregister.gov/api/v1/agencies/145","parent_id":null,"slug":"environmental-protection-agency"}],"excerpts":"revision addresses adjustments to the estimated time for activities and wage rates related to the <span class=\"match\">current</span> regulatory requirements as approved <span class=\"match\">under</span> OMB <span class=\"match\">Control</span> No. 2070-0202. In addition, the ICR revision addresses program changes related to the proposed amendments, including changes to content requirements for manufacturer-requested risk evaluation request and <span class=\"match\">associated</span> process changes. The estimated annual burden approved by OMB <span class=\"match\">under</span> OMB <span class=\"match\">Control</span> No. 2070-0231 is 166 hours. The total estimated annual respondent burden being proposed in the replacement"},{"title":"Clarifying Interstate Transportation of Firearms Under the Gun Control Act","type":"Proposed Rule","abstract":"The Bureau of Alcohol, Tobacco, Firearms, and Explosives (\"ATF\") proposes amending Department of Justice (\"Department\") regulations to clarify that, for purposes of transporting firearms interstate, any activities that are reasonably necessary to transportation such as staying overnight in temporary lodging, stopping for food, fuel, vehicle maintenance, an emergency, or medical treatment, or transiting between modes of transportation, are considered \"transport\" and thus protected by the Gun Control Act provision that addresses interstate transport of firearms. The proposed rule also addresses transporting ammunition and firearm accessories between states and the requirements for securing firearms during such transit.","document_number":"2026-08916","html_url":"https://www.federalregister.gov/documents/2026/05/06/2026-08916/clarifying-interstate-transportation-of-firearms-under-the-gun-control-act","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-05-06/pdf/2026-08916.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-08916.pdf?1777985128","publication_date":"2026-05-06","agencies":[{"raw_name":"DEPARTMENT OF JUSTICE","name":"Justice Department","id":268,"url":"https://www.federalregister.gov/agencies/justice-department","json_url":"https://www.federalregister.gov/api/v1/agencies/268","parent_id":null,"slug":"justice-department"},{"raw_name":"Bureau of Alcohol, Tobacco, Firearms, and Explosives","name":"Alcohol, Tobacco, Firearms, and Explosives Bureau","id":19,"url":"https://www.federalregister.gov/agencies/alcohol-tobacco-firearms-and-explosives-bureau","json_url":"https://www.federalregister.gov/api/v1/agencies/19","parent_id":268,"slug":"alcohol-tobacco-firearms-and-explosives-bureau"}],"excerpts":"the Treasury to the Department of Justice, <span class=\"match\">under</span> the general authority of the Attorney General. 26 U.S.C. 7801(a)(2); 28 U.S.C. 599A(c)(1). Thus, for ease of reference, this proposed rule refers to the Attorney General where relevant.\n \n \n \n \n 2 \n  In Attorney General Order Number 6353-2025, the Attorney General delegated authority to the Director to issue regulations pertaining to ATF's jurisdiction on those topics, including <span class=\"match\">under</span> the National Firearms Act, GCA, and Title XI of the Organized Crime <span class=\"match\">Control</span> Act. ATF's jurisdiction also includes those"},{"title":"Roof Control Plan Approval Criteria","type":"Proposed Rule","abstract":"MSHA is proposing to revise its roof control plan regulations to eliminate the provision that allows the District Manager to require additional measures to be included in plans. The current regulation may violate statutory authority; the Appointments Clause, by vesting significant regulatory authority in District Managers; and the Administrative Procedure Act (APA), by skipping notice and comment.","document_number":"2025-12230","html_url":"https://www.federalregister.gov/documents/2025/07/01/2025-12230/roof-control-plan-approval-criteria","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-07-01/pdf/2025-12230.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-12230.pdf?1751287526","publication_date":"2025-07-01","agencies":[{"raw_name":"DEPARTMENT OF LABOR","name":"Labor Department","id":271,"url":"https://www.federalregister.gov/agencies/labor-department","json_url":"https://www.federalregister.gov/api/v1/agencies/271","parent_id":null,"slug":"labor-department"},{"raw_name":"Mine Safety and Health Administration","name":"Mine Safety and Health Administration","id":288,"url":"https://www.federalregister.gov/agencies/mine-safety-and-health-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/288","parent_id":271,"slug":"mine-safety-and-health-administration"}],"excerpts":"approval of roof <span class=\"match\">control</span> plans. \n \n Type of Review: \n Substantive Change to <span class=\"match\">currently</span> approved information collection.\n \n \n OMB <span class=\"match\">Control</span> Number: \n 1219-0004.\n \n \n Title: \n Roof <span class=\"match\">Control</span> Plan for Underground Coal Mines.\n \n \n Description of the ICR: \n \n Background \n The proposed rule would apply to all underground coal mines. The existing rule allows the District Manager the discretion to revise roof <span class=\"match\">control</span> plans, while the proposed rule would decrease the burden <span class=\"match\">currently</span> faced by mine operators of having to revise their roof <span class=\"match\">control</span> plans when required"},{"title":"Medical Devices; Immunology and Microbiology Devices; Classification of the Device To Detect Nucleic Acids From Non-Viral Microorganism(s) Causing Sexually Transmitted Infections and Associated Resistance Marker(s)","type":"Rule","abstract":"The Food and Drug Administration (FDA, Agency, or we) is classifying the device to detect nucleic acids from non-viral microorganism(s) causing sexually transmitted infections and associated resistance marker(s) into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the device to detect nucleic acids from non-viral microorganism(s) causing sexually transmitted infections and associated resistance marker(s)'s classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.","document_number":"2025-08149","html_url":"https://www.federalregister.gov/documents/2025/05/09/2025-08149/medical-devices-immunology-and-microbiology-devices-classification-of-the-device-to-detect-nucleic","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-05-09/pdf/2025-08149.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-08149.pdf?1746708320","publication_date":"2025-05-09","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"regarding premarket approval, have been approved <span class=\"match\">under</span> OMB <span class=\"match\">control</span> number 0910-0231; the collections of information in part 807, subpart E, regarding premarket notification submissions, have been approved <span class=\"match\">under</span> OMB <span class=\"match\">control</span> number 0910-0120; the collections of information in 21 CFR part 820, regarding quality system regulation, have been approved <span class=\"match\">under</span> OMB <span class=\"match\">control</span> number 0910-0073; and the collections of information in 21 CFR parts 801 and 809, regarding labeling, have been approved <span class=\"match\">under</span> OMB <span class=\"match\">control</span> number 0910-0485. \n \n List of Subjects in 21 CFR"},{"title":"Schedules of Controlled Substances: Placement of Three Specific Fentanyl-Related Substances in Schedule I","type":"Proposed Rule","abstract":"The Drug Enforcement Administration proposes placing three fentanyl-related substances, as identified in this proposed rule, in schedule I of the Controlled Substances Act. These three substances fall within the definition of fentanyl-related substances set forth in the February 6, 2018 temporary scheduling order. Through the Temporary Reauthorization and Study of Emergency Scheduling of Fentanyl Analogues Act, which became law on February 6, 2020, Congress extended the temporary control of fentanyl-related substances until May 6, 2021. This temporary order was subsequently extended multiple times, most recently on March 15, 2025, which extended the order until September 30, 2025. If finalized, this action would make permanent the existing regulatory controls and administrative, civil, and criminal sanctions applicable to schedule I controlled substances on persons who handle (manufacture, distribute, import, export, engage in research, conduct instructional activities or chemical analysis, or possess), or propose to handle these three specific controlled substances.","document_number":"2025-10372","html_url":"https://www.federalregister.gov/documents/2025/06/10/2025-10372/schedules-of-controlled-substances-placement-of-three-specific-fentanyl-related-substances-in","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-06-10/pdf/2025-10372.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-10372.pdf?1749473109","publication_date":"2025-06-10","agencies":[{"raw_name":"DEPARTMENT OF JUSTICE","name":"Justice Department","id":268,"url":"https://www.federalregister.gov/agencies/justice-department","json_url":"https://www.federalregister.gov/api/v1/agencies/268","parent_id":null,"slug":"justice-department"},{"raw_name":"Drug Enforcement Administration","name":"Drug Enforcement Administration","id":116,"url":"https://www.federalregister.gov/agencies/drug-enforcement-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/116","parent_id":268,"slug":"drug-enforcement-administration"}],"excerpts":"this proposed rule meet the existing definition of fentanyl-related substances as they are not otherwise <span class=\"match\">controlled</span> in any other schedule (\n i.e., \n not included <span class=\"match\">under</span> another DEA <span class=\"match\">Controlled</span> Substance Code Number) and are structurally related to fentanyl by one or more of the five modifications listed <span class=\"match\">under</span> the definition. That temporary order was effective upon the date of publication. Pursuant to 21 U.S.C. 811(h)(2), the temporary <span class=\"match\">control</span> of fentanyl-related substances, a class of substances as defined in the order, as well as the three specific"},{"title":"Controlled Substances Ordering System (CSOS) Modernization","type":"Rule","abstract":"This rule is amending the Drug Enforcement Administration's (DEA) regulations to conform to the Controlled Substances Ordering System (CSOS) modernization effort by requiring all CSOS enrollment applications and supporting materials to be submitted through the Diversion Control Division secure online portal. These amendments improve the enrollment process by aligning it with DEA's current requirements for other online form submissions. The online submission of enrollment applications and supporting material through the secure online portal increases the efficiency of the enrollment, modification, and revocation processes, and ensures DEA's receipt of accurate documentation in a more timely and organized manner.","document_number":"2025-19325","html_url":"https://www.federalregister.gov/documents/2025/10/02/2025-19325/controlled-substances-ordering-system-csos-modernization","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-10-02/pdf/2025-19325.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-19325.pdf?1759322726","publication_date":"2025-10-02","agencies":[{"raw_name":"DEPARTMENT OF JUSTICE","name":"Justice Department","id":268,"url":"https://www.federalregister.gov/agencies/justice-department","json_url":"https://www.federalregister.gov/api/v1/agencies/268","parent_id":null,"slug":"justice-department"},{"raw_name":"Drug Enforcement Administration","name":"Drug Enforcement Administration","id":116,"url":"https://www.federalregister.gov/agencies/drug-enforcement-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/116","parent_id":268,"slug":"drug-enforcement-administration"}],"excerpts":"amendments allowed registrants to order schedule I and II <span class=\"match\">controlled</span> substances electronically and maintain records of these orders electronically. The intent of these amendments was to reduce paperwork and transaction times for DEA registrants who sell or buy <span class=\"match\">controlled</span> substances.\n \n \n \n 11 \n  \n Electronic Orders for <span class=\"match\">Controlled</span> Substances, \n 68 FR 38557 (June 27, 2003), and \n Electronic Orders for <span class=\"match\">Controlled</span> Substances, \n 70 FR 16901, (Apr. 1, 2005).\n \n \n Summary of <span class=\"match\">Current</span> CSOS Regulations \n The <span class=\"match\">current</span> CSOS regulations are found in 21 CFR parts 1305 and"},{"title":"Walking-Working Surfaces","type":"Proposed Rule","abstract":"This proposed rule removes a deadline in OSHA's Walking- Working Surfaces standard by which all fixed ladders that extend more than 24 feet above a lower level must be equipped with personal fall arrest systems or ladder safety systems. Additionally, OSHA is seeking comment on repealing or revising the requirement that employers use personal fall arrest systems on all fixed ladders over 24 feet tall and instead permitting employers to continue to use ladder cages or wells.","document_number":"2026-06578","html_url":"https://www.federalregister.gov/documents/2026/04/06/2026-06578/walking-working-surfaces","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-04-06/pdf/2026-06578.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-06578.pdf?1775220309","publication_date":"2026-04-06","agencies":[{"raw_name":"DEPARTMENT OF LABOR","name":"Labor Department","id":271,"url":"https://www.federalregister.gov/agencies/labor-department","json_url":"https://www.federalregister.gov/api/v1/agencies/271","parent_id":null,"slug":"labor-department"},{"raw_name":"Occupational Safety and Health Administration","name":"Occupational Safety and Health Administration","id":386,"url":"https://www.federalregister.gov/agencies/occupational-safety-and-health-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/386","parent_id":271,"slug":"occupational-safety-and-health-administration"}],"excerpts":"proposal.\n \n B. OMB Review <span class=\"match\">Under</span> the Paperwork Reduction Act of 1995 \n The Paperwork Reduction Act (PRA) defines “collection of information” to mean “the obtaining, causing to be obtained, soliciting, or requiring the disclosure to third parties or the public, of facts or opinions by or for an agency, regardless of form or format” (44 U.S.C. 3502(3)(A)). <span class=\"match\">Under</span> the PRA, a federal agency cannot conduct or sponsor a collection of information unless it is approved by OMB <span class=\"match\">under</span> the PRA and the agency displays a <span class=\"match\">currently</span> valid OMB <span class=\"match\">control</span> number (44 U.S.C. 3507)"},{"title":"Medicaid and Children's Health Insurance Program (CHIP) Generic Information Collection Activities: Proposed Collection; Comment Request","type":"Notice","abstract":"On May 28, 2010, the Office of Management and Budget (OMB) issued Paperwork Reduction Act (PRA) guidance related to the \"generic\" clearance process. Generally, this is an expedited process by which agencies may obtain OMB's approval of collection of information requests that are \"usually voluntary, low-burden, and uncontroversial collections,\" do not raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would fall under its umbrella. On October 23, 2011, OMB approved our initial request to use the generic clearance process under control number 0938-1148 (CMS-10398). It was last approved on April 26, 2021, via the standard PRA process which included the publication of 60- and 30-day Federal Register notices. The scope of the April 2021 umbrella accounts for Medicaid and CHIP State plan amendments, waivers, demonstrations, and reporting. This Federal Register notice seeks public comment on one or more of our collection of information requests that we believe are generic and fall within the scope of the umbrella. Interested persons are invited to submit comments regarding our burden estimates or any other aspect of this collection of information, including: the necessity and utility of the proposed information collection for the proper performance of the agency's functions, the accuracy of the estimated burden, ways to enhance the quality, utility and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden.","document_number":"2026-07803","html_url":"https://www.federalregister.gov/documents/2026/04/22/2026-07803/medicaid-and-childrens-health-insurance-program-chip-generic-information-collection-activities","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-04-22/pdf/2026-07803.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-07803.pdf?1776775512","publication_date":"2026-04-22","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Centers for Medicare & Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"}],"excerpts":"raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would <span class=\"match\">fall</span> <span class=\"match\">under</span> its umbrella. On October 23, 2011, OMB approved our initial request to use the generic clearance process <span class=\"match\">under</span> <span class=\"match\">control</span> number 0938-1148 (CMS-10398). It was last approved on April 26, 2021, via the standard PRA process which included the publication of 60- and 30-day \n Federal Register \n notices. The scope of the April 2021 umbrella"},{"title":"Medicaid and Children's Health Insurance Program (CHIP) Generic Information Collection Activities: Proposed Collection; Comment Request","type":"Notice","abstract":"On May 28, 2010, the Office of Management and Budget (OMB) issued Paperwork Reduction Act (PRA) guidance related to the \"generic\" clearance process. Generally, this is an expedited process by which agencies may obtain OMB's approval of collection of information requests that are \"usually voluntary, low-burden, and uncontroversial collections,\" do not raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would fall under its umbrella. On October 23, 2011, OMB approved our initial request to use the generic clearance process under control number 0938-1148 (CMS-10398). It was last approved on April 26, 2021, via the standard PRA process which included the publication of 60- and 30-day Federal Register notices. The scope of the April 2021 umbrella accounts for Medicaid and CHIP State plan amendments, waivers, demonstrations, and reporting. This Federal Register notice seeks public comment on one or more of our collection of information requests that we believe are generic and fall within the scope of the umbrella. Interested persons are invited to submit comments regarding our burden estimates or any other aspect of this collection of information, including: the necessity and utility of the proposed information collection for the proper performance of the agency's functions, the accuracy of the estimated burden, ways to enhance the quality, utility and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden.","document_number":"2026-10097","html_url":"https://www.federalregister.gov/documents/2026/05/20/2026-10097/medicaid-and-childrens-health-insurance-program-chip-generic-information-collection-activities","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-05-20/pdf/2026-10097.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-10097.pdf?1779194713","publication_date":"2026-05-20","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Centers for Medicare & Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"}],"excerpts":"raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would <span class=\"match\">fall</span> <span class=\"match\">under</span> its umbrella. On October 23, 2011, OMB approved our initial request to use the generic clearance process <span class=\"match\">under</span> <span class=\"match\">control</span> number 0938-1148 (CMS-10398). It was last approved on April 26, 2021, via the standard PRA process which included the publication of 60- and 30-day \n Federal Register \n notices. The scope of the April 2021 umbrella"},{"title":"Spring 2025 Semiannual Agenda of Regulations","type":"Notice","abstract":"In compliance with Executive Order 12866, entitled \"Regulatory Planning and Review,\" and the Regulatory Flexibility Act, as amended, the Department of Commerce (Commerce), in the spring and fall of each year, publishes in the Federal Register an agenda of regulations under development or review over the next 12 months. Rulemaking actions are grouped according to pre-rulemaking, proposed rules, final rules, long-term actions, and rulemaking actions completed since the publication of the Fall 2024 Unified Agenda. The purpose of the Agenda is to provide information to the public on regulations that are currently under review, being proposed, or recently issued by Commerce. It is expected that this information will enable the public to participate more effectively in Commerce's regulatory process. Commerce's Spring 2025 Unified Agenda includes regulatory activities that are expected to be conducted during the period July 1, 2025, through June 31, 2026.","document_number":"2025-18325","html_url":"https://www.federalregister.gov/documents/2025/09/22/2025-18325/spring-2025-semiannual-agenda-of-regulations","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-09-22/pdf/2025-18325.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-18325.pdf?1758285918","publication_date":"2025-09-22","agencies":[{"raw_name":"DEPARTMENT OF COMMERCE","name":"Commerce Department","id":54,"url":"https://www.federalregister.gov/agencies/commerce-department","json_url":"https://www.federalregister.gov/api/v1/agencies/54","parent_id":null,"slug":"commerce-department"},{"raw_name":"Office of the Secretary"}],"excerpts":"the Department of Commerce (Commerce), in the spring and <span class=\"match\">fall</span> of each year, publishes in the \n Federal Register \n an agenda of regulations <span class=\"match\">under</span> development or review over the next 12 months. Rulemaking actions are grouped according to pre-rulemaking, proposed rules, final rules, long-term actions, and rulemaking actions completed since the publication of the <span class=\"match\">Fall</span> 2024 Unified Agenda.\n \n The purpose of the Agenda is to provide information to the public on regulations that are <span class=\"match\">currently</span> <span class=\"match\">under</span> review, being proposed, or recently issued by Commerce."},{"title":"Medicaid and Children's Health Insurance Program (CHIP) Generic Information Collection Activities: Proposed Collection; Comment Request","type":"Notice","abstract":"On May 28, 2010, the Office of Management and Budget (OMB) issued Paperwork Reduction Act (PRA) guidance related to the \"generic\" clearance process. Generally, this is an expedited process by which agencies may obtain OMB's approval of collection of information requests that are \"usually voluntary, low-burden, and uncontroversial collections,\" do not raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would fall under its umbrella. On October 23, 2011, OMB approved our initial request to use the generic clearance process under control number 0938-1148 (CMS-10398). It was last approved on April 26, 2021, via the standard PRA process which included the publication of 60- and 30-day Federal Register notices. The scope of the April 2021 umbrella accounts for Medicaid and CHIP State plan amendments, waivers, demonstrations, and reporting. This Federal Register notice seeks public comment on one or more of our collection of information requests that we believe are generic and fall within the scope of the umbrella. Interested persons are invited to submit comments regarding our burden estimates or any other aspect of this collection of information, including: the necessity and utility of the proposed information collection for the proper performance of the agency's functions, the accuracy of the estimated burden, ways to enhance the quality, utility and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden.","document_number":"2025-22184","html_url":"https://www.federalregister.gov/documents/2025/12/08/2025-22184/medicaid-and-childrens-health-insurance-program-chip-generic-information-collection-activities","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-12-08/pdf/2025-22184.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-22184.pdf?1764942312","publication_date":"2025-12-08","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Centers for Medicare & Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"}],"excerpts":"raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would <span class=\"match\">fall</span> <span class=\"match\">under</span> its umbrella. On October 23, 2011, OMB approved our initial request to use the generic clearance process <span class=\"match\">under</span> <span class=\"match\">control</span> number 0938-1148 (CMS-10398). It was last approved on April 26, 2021, via the standard PRA process which included the publication of 60- and 30-day \n Federal Register \n notices. The scope of the April 2021 umbrella"},{"title":"Medicaid and Children's Health Insurance Program (CHIP) Generic Information Collection Activities: Proposed Collection; Comment Request","type":"Notice","abstract":"On May 28, 2010, the Office of Management and Budget (OMB) issued Paperwork Reduction Act (PRA) guidance related to the \"generic\" clearance process. Generally, this is an expedited process by which agencies may obtain OMB's approval of collection of information requests that are \"usually voluntary, low-burden, and uncontroversial collections,\" do not raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would fall under its umbrella. On October 23, 2011, OMB approved our initial request to use the generic clearance process under control number 0938-1148 (CMS-10398). It was last approved on April 26, 2021, via the standard PRA process which included the publication of 60- and 30-day Federal Register notices. The scope of the April 2021 umbrella accounts for Medicaid and CHIP State plan amendments, waivers, demonstrations, and reporting. This Federal Register notice seeks public comment on one or more of our collection of information requests that we believe are generic and fall within the scope of the umbrella. Interested persons are invited to submit comments regarding our burden estimates or any other aspect of this collection of information, including: the necessity and utility of the proposed information collection for the proper performance of the agency's functions, the accuracy of the estimated burden, ways to enhance the quality, utility and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden.","document_number":"2025-21124","html_url":"https://www.federalregister.gov/documents/2025/11/26/2025-21124/medicaid-and-childrens-health-insurance-program-chip-generic-information-collection-activities","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-11-26/pdf/2025-21124.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-21124.pdf?1764078316","publication_date":"2025-11-26","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Centers for Medicare & Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"}],"excerpts":"raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would <span class=\"match\">fall</span> <span class=\"match\">under</span> its umbrella. On October 23, 2011, OMB approved our initial request to use the generic clearance process <span class=\"match\">under</span> <span class=\"match\">control</span> number 0938-1148 (CMS-10398). It was last approved on April 26, 2021, via the standard PRA process which included the publication of 60- and 30-day \n Federal Register \n notices. The scope of the April 2021 umbrella"},{"title":"Medicaid and Children's Health Insurance Program (CHIP) Generic Information Collection Activities: Proposed Collection; Comment Request","type":"Notice","abstract":"On May 28, 2010, the Office of Management and Budget (OMB) issued Paperwork Reduction Act (PRA) guidance related to the \"generic\" clearance process. Generally, this is an expedited process by which agencies may obtain OMB's approval of collection of information requests that are \"usually voluntary, low-burden, and uncontroversial collections,\" do not raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would fall under its umbrella. This Federal Register notice seeks public comment on one or more of our collection of information requests that we believe are generic and fall within the scope of the umbrella. Interested persons are invited to submit comments regarding our burden estimates or any other aspect of this collection of information, including: the necessity and utility of the proposed information collection for the proper performance of the agency's functions, the accuracy of the estimated burden, ways to enhance the quality, utility and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden.","document_number":"2026-07802","html_url":"https://www.federalregister.gov/documents/2026/04/22/2026-07802/medicaid-and-childrens-health-insurance-program-chip-generic-information-collection-activities","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-04-22/pdf/2026-07802.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-07802.pdf?1776775511","publication_date":"2026-04-22","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Centers for Medicare & Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"}],"excerpts":"policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would <span class=\"match\">fall</span> <span class=\"match\">under</span> its umbrella. This \n Federal Register \n notice seeks public comment on one or more of our collection of information requests that we believe are generic and <span class=\"match\">fall</span> within the scope of the umbrella. Interested persons are invited to submit comments regarding our burden estimates or any other aspect of this collection of information, including: the necessity"},{"title":"Fall 2023 Semiannual Agenda of Regulations","type":"Proposed Rule","abstract":"In compliance with Executive Order 12866, entitled \"Regulatory Planning and Review,\" and the Regulatory Flexibility Act, as amended, the Department of Commerce (Commerce), in the spring and fall of each year, publishes in the Federal Register an agenda of regulations under development or review over the next 12 months. Rulemaking actions are grouped according to pre-rulemaking, proposed rules, final rules, long-term actions, and rulemaking actions completed since the spring 2023 agenda. The purpose of the Agenda is to provide information to the public on regulations that are currently under review, being proposed, or recently issued by Commerce. It is expected that this information will enable the public to participate more effectively in the Department's regulatory process. Commerce's fall 2023 regulatory agenda includes regulatory activities that are expected to be conducted during the period November 1, 2023, through October 31, 2024.","document_number":"2024-00451","html_url":"https://www.federalregister.gov/documents/2024/02/09/2024-00451/fall-2023-semiannual-agenda-of-regulations","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-02-09/pdf/2024-00451.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-00451.pdf?1707399914","publication_date":"2024-02-09","agencies":[{"raw_name":"DEPARTMENT OF COMMERCE","name":"Commerce Department","id":54,"url":"https://www.federalregister.gov/agencies/commerce-department","json_url":"https://www.federalregister.gov/api/v1/agencies/54","parent_id":null,"slug":"commerce-department"},{"raw_name":"Office of the Secretary"}],"excerpts":"as amended, the Department of Commerce (Commerce), in the spring and <span class=\"match\">fall</span> of each year, publishes in the \n Federal Register \n an agenda of regulations <span class=\"match\">under</span> development or review over the next 12 months. Rulemaking actions are grouped according to pre-rulemaking, proposed rules, final rules, long-term actions, and rulemaking actions completed since the spring 2023 agenda. The purpose of the Agenda is to provide information to the public on regulations that are <span class=\"match\">currently</span> <span class=\"match\">under</span> review, being proposed, or recently issued by Commerce. It is expected"},{"title":"Extension of Agency Information Collection Activity Under OMB Review: Airport Security Part 1542","type":"Notice","abstract":"This notice announces that the Transportation Security Administration (TSA) has forwarded the Information Collection Request (ICR), Office of Management and Budget (OMB) control number 1652-0002, abstracted below to OMB for review and approval of an extension of the currently approved collection under the Paperwork Reduction Act (PRA). The ICR describes the nature of the information collection and its expected burden. The collection includes requirements for airport operators to submit certain information to TSA, as well as to maintain and update records to ensure compliance with security provisions.","document_number":"2025-04551","html_url":"https://www.federalregister.gov/documents/2025/03/19/2025-04551/extension-of-agency-information-collection-activity-under-omb-review-airport-security-part-1542","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-03-19/pdf/2025-04551.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-04551.pdf?1742301922","publication_date":"2025-03-19","agencies":[{"raw_name":"DEPARTMENT OF HOMELAND SECURITY","name":"Homeland Security Department","id":227,"url":"https://www.federalregister.gov/agencies/homeland-security-department","json_url":"https://www.federalregister.gov/api/v1/agencies/227","parent_id":null,"slug":"homeland-security-department"},{"raw_name":"Transportation Security Administration","name":"Transportation Security Administration","id":494,"url":"https://www.federalregister.gov/agencies/transportation-security-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/494","parent_id":227,"slug":"transportation-security-administration"}],"excerpts":"Request: \n Extension of a <span class=\"match\">currently</span> approved collection.\n \n \n OMB <span class=\"match\">Control</span> Number: \n 1652-0002.\n \n \n Forms(s): \n NA.\n \n \n Affected Public: \n Airport operators.\n \n \n Abstract: \n The information collection is used to determine compliance with 49 CFR part 1542 and to ensure passenger safety and security by ensuring compliance with airport operator required security procedures. The following information collections and other recordkeeping requirements with which respondent covered airport operators must comply <span class=\"match\">fall</span> <span class=\"match\">under</span> this OMB <span class=\"match\">control</span> number: (1) development"},{"title":"Trichloroethylene (TCE); Regulation Under the Toxic Substances Control Act (TSCA)","type":"Rule","abstract":"The Environmental Protection Agency (EPA or Agency) is finalizing a rule to address the unreasonable risk of injury to health presented by trichloroethylene (TCE) under its conditions of use. TSCA requires that EPA address by rule any unreasonable risk of injury to health or the environment identified in a TSCA risk evaluation and apply requirements to the extent necessary so that the chemical no longer presents unreasonable risk. EPA's final rule will, among other things, prevent serious illness associated with uncontrolled exposures to the chemical by preventing consumer access to the chemical, restricting the industrial and commercial use of the chemical while also allowing for a reasonable transition period with interim worker protections in place where an industrial and commercial use of the chemical is being prohibited, and provide time-limited exemptions for critical or essential uses of TCE for which no technically and economically feasible safer alternatives are available.","document_number":"2024-29274","html_url":"https://www.federalregister.gov/documents/2024/12/17/2024-29274/trichloroethylene-tce-regulation-under-the-toxic-substances-control-act-tsca","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-12-17/pdf/2024-29274.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-29274.pdf?1734356718","publication_date":"2024-12-17","agencies":[{"raw_name":"ENVIRONMENTAL PROTECTION AGENCY","name":"Environmental Protection Agency","id":145,"url":"https://www.federalregister.gov/agencies/environmental-protection-agency","json_url":"https://www.federalregister.gov/api/v1/agencies/145","parent_id":null,"slug":"environmental-protection-agency"}],"excerpts":"finalizing a 10-year exemption <span class=\"match\">under</span> TSCA section 6(g) for DoD vessel requirements for potting, bonding and sealing compounds, and bonding and cleaning requirements for naval combat systems, radars, sensors, equipment, and fabrication and prototyping processes. Additionally, EPA is finalizing a 50-year exemption <span class=\"match\">under</span> TSCA section 6(g) for the industrial and commercial use of TCE for critical laboratory activities; for example, laboratory activities <span class=\"match\">associated</span> with ongoing environmental cleanup projects that <span class=\"match\">fall</span> <span class=\"match\">under</span> the Superfund program or other"},{"title":"Medicaid and Children's Health Insurance Program (CHIP) Generic Information Collection Activities: Proposed Collection; Comment Request","type":"Notice","abstract":"On May 28, 2010, the Office of Management and Budget (OMB) issued Paperwork Reduction Act (PRA) guidance related to the \"generic\" clearance process. Generally, this is an expedited process by which agencies may obtain OMB's approval of collection of information requests that are \"usually voluntary, low-burden, and uncontroversial collections,\" do not raise any substantive or policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would fall under its umbrella. This Federal Register notice seeks public comment on one or more of our collection of information requests that we believe are generic and fall within the scope of the umbrella. Interested persons are invited to submit comments regarding our burden estimates or any other aspect of this collection of information, including: the necessity and utility of the proposed information collection for the proper performance of the agency's functions, the accuracy of the estimated burden, ways to enhance the quality, utility and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden.","document_number":"2025-17121","html_url":"https://www.federalregister.gov/documents/2025/09/08/2025-17121/medicaid-and-childrens-health-insurance-program-chip-generic-information-collection-activities","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-09-08/pdf/2025-17121.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-17121.pdf?1757076312","publication_date":"2025-09-08","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Centers for Medicare & Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"}],"excerpts":"policy issues, and do not require policy or methodological review. The process requires the submission of an overarching plan that defines the scope of the individual collections that would <span class=\"match\">fall</span> <span class=\"match\">under</span> its umbrella. This \n Federal Register \n notice seeks public comment on one or more of our collection of information requests that we believe are generic and <span class=\"match\">fall</span> within the scope of the umbrella. Interested persons are invited to submit comments regarding our burden estimates or any other aspect of this collection of information, including: the necessity"}]}