{"description":"Documents matching 'publishing proposed designation provide public'","count":9309,"total_pages":50,"next_page_url":"https://www.federalregister.gov/api/v1/documents?conditions%5Bterm%5D=publishing+proposed+designation+provide+public&format=json&page=2","results":[{"title":"Proposed Designation of Database to the Do Not Pay Working System","type":"Notice","abstract":"The Payment Integrity Information Act of 2019 (PIIA) authorizes the Office of Management and Budget (OMB) to designate databases for inclusion in the U.S. Department of the Treasury (Treasury) Do Not Pay Working System under the Do Not Pay Initiative. PIIA requires OMB to provide public notice and an opportunity for comment prior to designating databases. In fulfillment of this requirement, OMB is publishing this Notice of Proposed Designation to provide the public an opportunity to comment on the proposed designation of the U.S. Department of Veterans Affairs (VA) Benefits Enterprise Platform (BEP) database for use in the Do Not Pay Working System with the Public Assistance Reporting Information System (PARIS). This notice has a 15-day comment period.","document_number":"2025-11557","html_url":"https://www.federalregister.gov/documents/2025/06/24/2025-11557/proposed-designation-of-database-to-the-do-not-pay-working-system","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-06-24/pdf/2025-11557.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-11557.pdf?1750682713","publication_date":"2025-06-24","agencies":[{"raw_name":"OFFICE OF MANAGEMENT AND BUDGET","name":"Management and Budget Office","id":280,"url":"https://www.federalregister.gov/agencies/management-and-budget-office","json_url":"https://www.federalregister.gov/api/v1/agencies/280","parent_id":null,"slug":"management-and-budget-office"}],"excerpts":"ACTION: \n Notice of <span class=\"match\">proposed</span> <span class=\"match\">designation</span>. \n \n \n SUMMARY: \n \n The Payment Integrity Information Act of 2019 (PIIA) authorizes the Office of Management and Budget (OMB) to designate databases for inclusion in the U.S. Department of the Treasury (Treasury) Do Not Pay Working System under the Do Not Pay Initiative. PIIA requires OMB to <span class=\"match\">provide</span> <span class=\"match\">public</span> notice and an opportunity for comment prior to designating databases. In fulfillment of this requirement, OMB is <span class=\"match\">publishing</span> this Notice of <span class=\"match\">Proposed</span> <span class=\"match\">Designation</span> to <span class=\"match\">provide</span> the <span class=\"match\">public</span> an opportunity to comment"},{"title":"Proposed Designation of Databases to the Do Not Pay Working System","type":"Notice","abstract":"The Payment Integrity Information Act of 2019 (PIIA) authorizes the Office of Management and Budget (OMB) to designate additional databases for inclusion in the Department of the Treasury (Treasury) Do Not Pay Working System under the Do Not Pay Initiative. PIIA requires OMB to provide public notice and an opportunity for comment prior to designating additional databases. In fulfillment of this requirement, OMB is publishing this Notice of Proposed Designation to provide the public an opportunity to comment on the proposed designation of: Treasury's Account Verification Services (AVS); and Treasury's Death Notification Entries (DNE). This notice has a 30-day comment period.","document_number":"2024-18689","html_url":"https://www.federalregister.gov/documents/2024/08/29/2024-18689/proposed-designation-of-databases-to-the-do-not-pay-working-system","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-08-29/pdf/2024-18689.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-18689.pdf?1724849113","publication_date":"2024-08-29","agencies":[{"raw_name":"OFFICE OF MANAGEMENT AND BUDGET","name":"Management and Budget Office","id":280,"url":"https://www.federalregister.gov/agencies/management-and-budget-office","json_url":"https://www.federalregister.gov/api/v1/agencies/280","parent_id":null,"slug":"management-and-budget-office"}],"excerpts":"\n Notice of <span class=\"match\">proposed</span> <span class=\"match\">designation</span>. \n \n \n SUMMARY: \n The Payment Integrity Information Act of 2019 (PIIA) authorizes the Office of Management and Budget (OMB) to designate additional databases for inclusion in the Department of the Treasury (Treasury) Do Not Pay Working System under the Do Not Pay Initiative. PIIA requires OMB to <span class=\"match\">provide</span> <span class=\"match\">public</span> notice and an opportunity for comment prior to designating additional databases. In fulfillment of this requirement, OMB is <span class=\"match\">publishing</span> this Notice of <span class=\"match\">Proposed</span> <span class=\"match\">Designation</span> to <span class=\"match\">provide</span> the <span class=\"match\">public</span> an opportunity"},{"title":"Removal of Regulations for Renewal Communities Designations","type":"Rule","abstract":"This rule removes HUD's Renewal Communities regulations because the designations were time limited, and all incentives have been repealed and sunset.","document_number":"2026-04447","html_url":"https://www.federalregister.gov/documents/2026/03/06/2026-04447/removal-of-regulations-for-renewal-communities-designations","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-03-06/pdf/2026-04447.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-04447.pdf?1772718314","publication_date":"2026-03-06","agencies":[{"raw_name":"DEPARTMENT OF HOUSING AND URBAN DEVELOPMENT","name":"Housing and Urban Development Department","id":228,"url":"https://www.federalregister.gov/agencies/housing-and-urban-development-department","json_url":"https://www.federalregister.gov/api/v1/agencies/228","parent_id":null,"slug":"housing-and-urban-development-department"}],"excerpts":"24 CFR part 10 <span class=\"match\">provides</span> narrow exceptions to the notice and comment requirements if the Department finds good cause to omit notice and <span class=\"match\">public</span> participation. The good cause requirement under 24 CFR 10.1 may be satisfied when notice and <span class=\"match\">public</span> comment are impracticable, unnecessary, or contrary to the <span class=\"match\">public</span> interest. To publish a rule prior to receiving and responding to <span class=\"match\">public</span> comments, the agency must find that at least one good cause exceptions is applicable. \n HUD has determined that good cause exists to promulgate this final rule without prior"},{"title":"Draft Designation of National Multimodal Freight Network and State Input Process","type":"Notice","abstract":"The U.S. Department of Transportation (DOT or Department) is publishing a draft designation of the National Multimodal Freight Network (NMFN or Network) as required Federal law. The designation is informed by the comments received on a notice published by DOT on April 12, 2024. DOT is also using this notice to request comments or proposed modifications to the draft Network prior to designating the Network. Once the Network is designated by DOT, States will have the opportunity to submit additional designations through the \"State Input\" process required by statute.","document_number":"2025-00474","html_url":"https://www.federalregister.gov/documents/2025/01/13/2025-00474/draft-designation-of-national-multimodal-freight-network-and-state-input-process","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-01-13/pdf/2025-00474.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-00474.pdf?1736516732","publication_date":"2025-01-13","agencies":[{"raw_name":"DEPARTMENT OF TRANSPORTATION","name":"Transportation Department","id":492,"url":"https://www.federalregister.gov/agencies/transportation-department","json_url":"https://www.federalregister.gov/api/v1/agencies/492","parent_id":null,"slug":"transportation-department"},{"raw_name":"Office of the Secretary"}],"excerpts":"will be required to certify their additional <span class=\"match\">designations</span> meet the requirements of statute. DOT anticipates providing States with an extended period of no less than 180 days to make these <span class=\"match\">designations</span>. \n DOT is required to redesignate the NMFN within 5 years after the initial <span class=\"match\">designation</span>, and every 5 years thereafter. \n Schedule \n DOT is requesting comments, feedback, and <span class=\"match\">proposed</span> modifications within 45 days of publication of this Notice. \n <span class=\"match\">Public</span> Comment \n \n DOT will accept written comments on the <span class=\"match\">public</span> docket associated with this notice. If commenters"},{"title":"Procedures for Supervisory Designation Proceedings","type":"Rule","abstract":"The Consumer Financial Protection Bureau (CFPB or Bureau) is rescinding the amendments it adopted in April 2022, November 2022, and April 2024, to the Procedures for Supervisory Designation Proceedings, with the exception of some limited process adjustments.","document_number":"2025-18622","html_url":"https://www.federalregister.gov/documents/2025/09/25/2025-18622/procedures-for-supervisory-designation-proceedings","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-09-25/pdf/2025-18622.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-18622.pdf?1758717921","publication_date":"2025-09-25","agencies":[{"raw_name":"Consumer Financial Protection Bureau","name":"Consumer Financial Protection Bureau","id":573,"url":"https://www.federalregister.gov/agencies/consumer-financial-protection-bureau","json_url":"https://www.federalregister.gov/api/v1/agencies/573","parent_id":null,"slug":"consumer-financial-protection-bureau"}],"excerpts":"members include installment lenders submitted comments opposing any <span class=\"match\">public</span> release of decisions and orders. Accordingly, they supported the Bureau's <span class=\"match\">proposed</span> rescission. All three of these trade associations cited unfair reputational harm from <span class=\"match\">public</span> release. Two associations identified a risk to competition, because firms that contest <span class=\"match\">designation</span> may be competitively disadvantaged by a <span class=\"match\">public</span> order compared to firms that consent to <span class=\"match\">designation</span> and so are not the focus of a <span class=\"match\">public</span> order. Also, if a published order raises concerns about a particular"},{"title":"Agency Information Collection Activities; Proposed Collection; Comment Request; Current Good Manufacturing Practice (CGMP): Manufacturing, Processing, Packing, and Holding of Drugs; GMP for Finished Pharmaceuticals (Including Active Pharmaceutical Ingredients) and the Advanced Manufacturing Technologies Designation Program","type":"Notice","abstract":"The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the information collection associated with CGMP for drugs, finished pharmaceuticals, including active pharmaceutical ingredients (APIs), and the advanced manufacturing technologies (AMT) designation program.","document_number":"2026-03326","html_url":"https://www.federalregister.gov/documents/2026/02/20/2026-03326/agency-information-collection-activities-proposed-collection-comment-request-current-good","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-02-20/pdf/2026-03326.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-03326.pdf?1771508709","publication_date":"2026-02-20","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":"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":"requests or requirements that members of the <span class=\"match\">public</span> submit reports, keep records, or <span class=\"match\">provide</span> information to a third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires Federal Agencies to <span class=\"match\">provide</span> a 60-day notice in the \n Federal Register \n concerning each <span class=\"match\">proposed</span> collection of information, including each <span class=\"match\">proposed</span> extension of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, FDA is <span class=\"match\">publishing</span> notice of the <span class=\"match\">proposed</span> collection of information set forth in"},{"title":"Periodic Review of the Designations of the Mechanical Licensing Collective and Digital Licensee Coordinator","type":"Notice","abstract":"The U.S. Copyright Office, as required by the Music Modernization Act, has completed its first periodic review of the existing designations of the mechanical licensing collective and digital licensee coordinator and has determined that both designations should be continued.","document_number":"2026-11117","html_url":"https://www.federalregister.gov/documents/2026/06/03/2026-11117/periodic-review-of-the-designations-of-the-mechanical-licensing-collective-and-digital-licensee","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-03/pdf/2026-11117.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-11117.pdf?1780404320","publication_date":"2026-06-03","agencies":[{"raw_name":"LIBRARY OF CONGRESS","name":"Library of Congress","id":277,"url":"https://www.federalregister.gov/agencies/library-of-congress","json_url":"https://www.federalregister.gov/api/v1/agencies/277","parent_id":null,"slug":"library-of-congress"},{"raw_name":"Copyright Office","name":"Copyright Office, Library of Congress","id":87,"url":"https://www.federalregister.gov/agencies/copyright-office-library-of-congress","json_url":"https://www.federalregister.gov/api/v1/agencies/87","parent_id":277,"slug":"copyright-office-library-of-congress"}],"excerpts":"https://www.copyright.gov/rulemaking/mma-<span class=\"match\">designations</span>/ex-parte-communications.html \n (last visited May 26, 2026) (hosting \n ex parte \n meeting summary letters related to the Office's initial <span class=\"match\">designations</span>).\n \n \n \n \n 26 \n  Initial <span class=\"match\">Designation</span> at 32292, 32296; 37 CFR 210.23.\n \n \n \n \n 27 \n  Initial <span class=\"match\">Designation</span> at 32276, 32296.\n \n \n \n \n 28 \n  37 CFR 210.23; Initial <span class=\"match\">Designation</span> at 32296.\n \n \n 2. First Periodic Review \n \n On January 30, 2024, the Office issued an NOI regarding the periodic review of the <span class=\"match\">designations</span>.\n 29 \n \n The currently designated mechanical"},{"title":"Designation-Restrict the Operation of Unmanned Aircraft in Close Proximity to a Fixed Site Facility; Extension of Comment Period","type":"Proposed Rule","abstract":"This action extends the comment period for the NPRM titled \"Designation--Restrict the Operation of Unmanned Aircraft in Close Proximity to a Fixed Site Facility\" that was published in the Federal Register on May 6, 2026, to allow commenters additional time to analyze the proposed rule and prepare a response. In the NPRM, FAA proposed a process for operators and proprietors of certain fixed site facilities to request an unmanned aircraft flight restriction (UAFR); criteria to demonstrate the UAFR is necessary for: aviation safety, protection of people and property on the ground, national security, or homeland security; and identified the types of operations allowed in the UAFR.","document_number":"2026-13126","html_url":"https://www.federalregister.gov/documents/2026/06/30/2026-13126/designation-restrict-the-operation-of-unmanned-aircraft-in-close-proximity-to-a-fixed-site-facility","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-30/pdf/2026-13126.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-13126.pdf?1782486908","publication_date":"2026-06-30","agencies":[{"raw_name":"DEPARTMENT OF TRANSPORTATION","name":"Transportation Department","id":492,"url":"https://www.federalregister.gov/agencies/transportation-department","json_url":"https://www.federalregister.gov/api/v1/agencies/492","parent_id":null,"slug":"transportation-department"},{"raw_name":"Federal Aviation Administration","name":"Federal Aviation Administration","id":159,"url":"https://www.federalregister.gov/agencies/federal-aviation-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/159","parent_id":492,"slug":"federal-aviation-administration"}],"excerpts":"ACTION: \n Notice of <span class=\"match\">proposed</span> rulemaking (NPRM); extension of comment period. \n \n \n SUMMARY: \n \n This action extends the comment period for the NPRM titled “<span class=\"match\">Designation</span>—Restrict the Operation of Unmanned Aircraft in Close Proximity to a Fixed Site Facility” that was published in the \n Federal Register \n on May 6, 2026, to allow commenters additional time to analyze the <span class=\"match\">proposed</span> rule and prepare a response. In the NPRM, FAA <span class=\"match\">proposed</span> a process for operators and proprietors of certain fixed site facilities to request an unmanned aircraft flight restriction"},{"title":"Agency Information Collection Activities; Proposed Collection; Comment Request; New Animal Drugs for Minor Use and Minor Species","type":"Notice","abstract":"The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the information collection associated with designation of new animal drugs for minor use and minor species and indexing of new animal drugs for minor species.","document_number":"2026-03353","html_url":"https://www.federalregister.gov/documents/2026/02/20/2026-03353/agency-information-collection-activities-proposed-collection-comment-request-new-animal-drugs-for","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-02-20/pdf/2026-03353.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-03353.pdf?1771508712","publication_date":"2026-02-20","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":"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":"requests or requirements that members of the <span class=\"match\">public</span> submit reports, keep records, or <span class=\"match\">provide</span> information to a third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires Federal Agencies to <span class=\"match\">provide</span> a 60-day notice in the \n Federal Register \n concerning each <span class=\"match\">proposed</span> collection of information, including each <span class=\"match\">proposed</span> extension of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, FDA is <span class=\"match\">publishing</span> notice of the <span class=\"match\">proposed</span> collection of information set forth in"},{"title":"Designation of Phenethyl Halides as List I Chemicals","type":"Proposed Rule","abstract":"The Drug Enforcement Administration is proposing the control of phenethyl halides as list I chemicals under the Controlled Substances Act (CSA). Phenethyl halides are important to the illicit manufacture of fentanyl, as well as fentanyl analogues, and fentanyl- related substances as they are often used in synthetic routes to manufacture these substances. Further, in the respective synthetic routes in which they are used to manufacture fentanyl, fentanyl analogues, and fentanyl-related substances, various phenethyl halides, such as phenethyl bromide and phenethyl chloride, can be substituted for each other. If finalized, the proposed rule would subject handlers of phenethyl halides to the chemical regulatory provisions of the CSA and its implementing regulations. This proposed rulemaking does not establish a threshold for domestic and international transactions of phenethyl halides. As such, all transactions of phenethyl halides regardless of size or concentration, shall be regulated and would be subject to control under the CSA.","document_number":"2026-13825","html_url":"https://www.federalregister.gov/documents/2026/07/09/2026-13825/designation-of-phenethyl-halides-as-list-i-chemicals","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-07-09/pdf/2026-13825.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-13825.pdf?1783514708","publication_date":"2026-07-09","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":"and fentanyl analogous substances, the <span class=\"match\">proposed</span> rule, if finalized, will regulate, in addition to manufacturing, the distribution, import, and export of phenethyl halides. As such, DEA believes the <span class=\"match\">proposed</span> controls will help mitigate the access and illegal distribution of these substances to manufacture fentanyl and analogous substances.\n \n <span class=\"match\">Proposed</span> <span class=\"match\">Designation</span> of Phenethyl Halides as List I Chemicals \n The CSA, specifically 21 U.S.C. 802(34), and its implementing regulations at 21 CFR 1310.02(c), <span class=\"match\">provide</span> the Attorney General with the authority"},{"title":"Platform Technology Designation Program; Draft Guidance for Industry; Availability; Agency Information Collection Activities; Proposed Collection; Comment Request","type":"Notice","abstract":"The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a draft guidance for industry entitled \"Platform Technology Designation Program for Drug Development.\" The purpose of this draft guidance is to provide details about the implementation of the Platform Technology Designation Program established by the PREVENT Pandemics Act. This draft guidance outlines eligibility factors for receiving a platform technology designation, potential benefits of receiving a designation, how to leverage data from designated platform technologies, how to discuss the planned designation request as part of a milestone meeting, the recommended content of a designation request submission, and the review timelines for a designation request. This draft guidance, when finalized, will represent the current thinking of FDA.","document_number":"2024-11686","html_url":"https://www.federalregister.gov/documents/2024/05/29/2024-11686/platform-technology-designation-program-draft-guidance-for-industry-availability-agency-information","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-05-29/pdf/2024-11686.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-11686.pdf?1716900318","publication_date":"2024-05-29","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":"Technology <span class=\"match\">Designation</span> Program for Drug Development.” The purpose of this draft guidance is to <span class=\"match\">provide</span> details about the implementation of the Platform Technology <span class=\"match\">Designation</span> Program established by the PREVENT Pandemics Act. This draft guidance outlines eligibility factors for receiving a platform technology <span class=\"match\">designation</span>, potential benefits of receiving a <span class=\"match\">designation</span>, how to leverage data from designated platform technologies, how to discuss the planned <span class=\"match\">designation</span> request as part of a milestone meeting, the recommended content of a <span class=\"match\">designation</span> request"},{"title":"Proposed Data Collection Submitted for Public Comment and Recommendations","type":"Notice","abstract":"The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other federal agencies the opportunity to comment on a continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled the Million Hearts[supreg] Hypertension Control Challenge. This program is a national initiative to prevent one million heart attacks and strokes by 2027.","document_number":"2025-10904","html_url":"https://www.federalregister.gov/documents/2025/06/16/2025-10904/proposed-data-collection-submitted-for-public-comment-and-recommendations","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-06-16/pdf/2025-10904.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-10904.pdf?1749818718","publication_date":"2025-06-16","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 Disease Control and Prevention","name":"Centers for Disease Control and Prevention","id":44,"url":"https://www.federalregister.gov/agencies/centers-for-disease-control-and-prevention","json_url":"https://www.federalregister.gov/api/v1/agencies/44","parent_id":221,"slug":"centers-for-disease-control-and-prevention"}],"excerpts":"conduct or sponsor. In addition, the PRA also requires federal agencies to <span class=\"match\">provide</span> a 60-day notice in the \n Federal Register \n concerning each <span class=\"match\">proposed</span> collection of information, including each new <span class=\"match\">proposed</span> collection, each <span class=\"match\">proposed</span> extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are <span class=\"match\">publishing</span> this notice of a <span class=\"match\">proposed</span> data collection as described below.\n \n The OMB is particularly interested"},{"title":"Public Briefing on Revisions to Space-Related Export Controls Under Export Administration Regulations and International Traffic in Arms Regulations","type":"Proposed Rule","abstract":"On October 23, 2024, the Bureau of Industry and Security (BIS) published in the Federal Register a proposed rule, \"Export Administration Regulations: Revisions to Space-Related Export Controls, including Addition of License Exception Commercial Space Activities (CSA).\" On the same day, the State Department's Directorate of Defense Trade Controls (DDTC) published in the Federal Register a proposed rule, \"International Traffic in Arms Regulations (ITAR): U.S. Munitions List Categories IV and XV.\" This document announces that, on November 6, 2024, BIS will host a public briefing on these proposed rules. This document also provides details on the procedures for participating in the public briefing. Elsewhere in this issue of the Federal Register, BIS is publishing notification of the public briefing on related final rules.","document_number":"2024-25715","html_url":"https://www.federalregister.gov/documents/2024/11/05/2024-25715/public-briefing-on-revisions-to-space-related-export-controls-under-export-administration","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-11-05/pdf/2024-25715.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-25715.pdf?1730465135","publication_date":"2024-11-05","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":"Bureau of Industry and Security","name":"Industry and Security Bureau","id":241,"url":"https://www.federalregister.gov/agencies/industry-and-security-bureau","json_url":"https://www.federalregister.gov/api/v1/agencies/241","parent_id":54,"slug":"industry-and-security-bureau"}],"excerpts":"Categories IV and XV.” This document announces that, on November 6, 2024, BIS will host a <span class=\"match\">public</span> briefing on these <span class=\"match\">proposed</span> rules. This document also <span class=\"match\">provides</span> details on the procedures for participating in the <span class=\"match\">public</span> briefing. Elsewhere in this issue of the \n Federal Register \n , BIS is <span class=\"match\">publishing</span> notification of the <span class=\"match\">public</span> briefing on related final rules.\n \n \n \n DATES: \n \n \n <span class=\"match\">Public</span> briefing: \n The <span class=\"match\">public</span> briefing will be held on November 6, 2024. The <span class=\"match\">public</span> briefing will begin at 1 p.m. Eastern Standard Time (EST) and conclude at 3 p.m. EST.\n \n"},{"title":"Agency Information Collection Activities; Proposed Collection; Comment Request; Orphan Drugs","type":"Notice","abstract":"The Food and Drug Administration (FDA, Agency, or we) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on information collection associated with orphan drug requirements.","document_number":"2026-07423","html_url":"https://www.federalregister.gov/documents/2026/04/16/2026-07423/agency-information-collection-activities-proposed-collection-comment-request-orphan-drugs","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-04-16/pdf/2026-07423.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-07423.pdf?1776257122","publication_date":"2026-04-16","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":"requests or requirements that members of the <span class=\"match\">public</span> submit reports, keep records, or <span class=\"match\">provide</span> information to a third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires Federal Agencies to <span class=\"match\">provide</span> a 60-day notice in the \n Federal Register \n concerning each <span class=\"match\">proposed</span> collection of information, including each <span class=\"match\">proposed</span> extension of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, FDA is <span class=\"match\">publishing</span> notice of the <span class=\"match\">proposed</span> collection of information set forth in"},{"title":"Medicare Program; Ensuring Safety Through Domestic Security With Made in America Personal Protective Equipment (PPE) and Essential Medicine Procurement by Medicare Participating Hospitals","type":"Proposed Rule","abstract":"This advance notice of proposed rulemaking solicits public comment on potential options we may consider for Medicare participating hospitals to help foster a more resilient supply chain for American- made personal protective equipment and essential medicines to secure our nation's health and safety and to reflect the additional resource costs incurred when procuring these domestically manufactured items. We seek input on a possible new \"Secure American Medical Supplies\" friendly designation that could be earned by hospitals that demonstrate their commitment to domestic procurement. In addition, we seek input on potential ways such a designation could facilitate the creation of new, streamlined payment policies to support hospitals in their efforts. We are also seeking input on a potential new structural quality measure as part of the Hospital Inpatient Quality Reporting (IQR) Program that could promote hospital commitments to invest in domestic procurement to secure our nation's health and safety.","document_number":"2026-01730","html_url":"https://www.federalregister.gov/documents/2026/01/29/2026-01730/medicare-program-ensuring-safety-through-domestic-security-with-made-in-america-personal-protective","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-01-29/pdf/2026-01730.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-01730.pdf?1769465709","publication_date":"2026-01-29","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":"Where would it be most helpful for this <span class=\"match\">designation</span> to appear? What would be the most appropriate entity to grant this <span class=\"match\">designation</span>? What other ways might be effective? \n • For administering the <span class=\"match\">designation</span>, what are potentially useful alternatives to self-attestation? How could hospitals be asked to <span class=\"match\">provide</span> proof that they purchased from domestic suppliers? Could hospital accreditors, group purchasing organizations (GPOs) or some other entity be better positioned to administer oversight of the <span class=\"match\">designation</span>? \n • What is the most appropriate definition"},{"title":"Endangered and Threatened Wildlife and Plants; Endangered Species Status for Black Creek Crayfish and Designation of Critical Habitat","type":"Proposed Rule","abstract":"We, the U.S. Fish and Wildlife Service (Service), propose to list the Black Creek crayfish (Procambarus pictus), a crayfish species from Florida, as an endangered species under the Endangered Species Act of 1973, as amended (Act). We also propose to designate critical habitat for the Black Creek crayfish under the Act. In total, approximately 1,056 kilometers (656 miles) of streams in Clay, Duval, Putnam, and St. Johns Counties, Florida, fall within the boundaries of the proposed critical habitat designation. If we finalize this rule as proposed, it would extend the Act's protections to this species and its designated critical habitat. We also announce the availability of an economic analysis of the proposed critical habitat designation for the Black Creek crayfish.","document_number":"2024-20106","html_url":"https://www.federalregister.gov/documents/2024/09/10/2024-20106/endangered-and-threatened-wildlife-and-plants-endangered-species-status-for-black-creek-crayfish-and","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-09-10/pdf/2024-20106.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-20106.pdf?1725885917","publication_date":"2024-09-10","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":"Fish and Wildlife Service","name":"Fish and Wildlife Service","id":197,"url":"https://www.federalregister.gov/agencies/fish-and-wildlife-service","json_url":"https://www.federalregister.gov/api/v1/agencies/197","parent_id":253,"slug":"fish-and-wildlife-service"}],"excerpts":"boundaries shown on the maps of this <span class=\"match\">proposed</span> rule have been excluded by text in the <span class=\"match\">proposed</span> rule and are not <span class=\"match\">proposed</span> for <span class=\"match\">designation</span> as critical habitat. Therefore, if the critical habitat is finalized as <span class=\"match\">proposed</span>, a Federal action involving these lands would not trigger section 7 consultation with respect to critical habitat and the requirement of no adverse modification unless the specific action would affect the physical or biological features in the adjacent critical habitat. \n Units are <span class=\"match\">proposed</span> for <span class=\"match\">designation</span> based on one or more of the physical"},{"title":"Designation of P2P Methyl Glycidic Acid as a List I Chemical","type":"Proposed Rule","abstract":"The Drug Enforcement Administration is proposing the control of the chemical 2-methyl-3-phenyloxirane-2-carboxylic acid (also known as P2P methyl glycidic acid and BMK glycidic acid) and its esters, its optical and geometric isomers, its salts, salts of its optical and geometric isomers and its esters, and any combination thereof, whenever the existence of such is possible, as a list I chemical under the Controlled Substances Act (CSA). P2P methyl glycidic acid is important to the manufacture of the schedule II controlled substances phenylacetone (also known as phenyl-2-propanone or P2P), methamphetamine, and amphetamine, and it is used in clandestine laboratories to illicitly manufacture these controlled substances. If finalized, this proposed rule would subject handlers of P2P methyl glycidic acid to the chemical regulatory provisions of the CSA and its implementing regulations. This rulemaking does not establish a threshold for domestic and international transactions of P2P methyl glycidic acid. As such, all transactions of P2P methyl glycidic acid, regardless of size, shall be regulated. In addition, chemical mixtures containing P2P methyl glycidic acid are not exempt from regulatory requirements at any concentration. Therefore, all transactions of chemical mixtures containing any quantity of P2P methyl glycidic acid shall be regulated pursuant to the CSA. However, manufacturers may submit an application for exemption for those mixtures that do not qualify for automatic exemption.","document_number":"2025-19384","html_url":"https://www.federalregister.gov/documents/2025/10/02/2025-19384/designation-of-p2p-methyl-glycidic-acid-as-a-list-i-chemical","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-10-02/pdf/2025-19384.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-19384.pdf?1759322732","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":"Drug Enforcement Administration; Telephone: (571) 362- 3249. As required by 5 U.S.C. 553(b)(4), a summary of this <span class=\"match\">proposed</span> rule may be found in the docket for this rulemaking at \n http://www.regulations.gov. \n \n \n \n \n SUPPLEMENTARY INFORMATION: \n Posting of <span class=\"match\">Public</span> Comments \n \n Please note that all comments received in response to this docket are considered part of the <span class=\"match\">public</span> record. DEA generally will make comments available for <span class=\"match\">public</span> inspection online at \n http://www.regulations.gov. \n Such information includes personal or business identifiers (such"},{"title":"Designation of Propionyl Chloride as a List I Chemical","type":"Rule","abstract":"The Drug Enforcement Administration is finalizing the control of propionyl chloride as a list I chemical under the Controlled Substances Act (CSA). Propionyl chloride is used in the illicit manufacture of the controlled substances fentanyl, fentanyl analogues, and fentanyl-related substances, and it is important to the manufacture of these substances. This final rule subjects handlers of propionyl chloride to the chemical regulatory provisions of the CSA and its implementing regulations.","document_number":"2026-04657","html_url":"https://www.federalregister.gov/documents/2026/03/10/2026-04657/designation-of-propionyl-chloride-as-a-list-i-chemical","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-03-10/pdf/2026-04657.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-04657.pdf?1773060313","publication_date":"2026-03-10","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":" 2007).\n \n \n \n \n 10 \n  \n <span class=\"match\">Designation</span> of Benzylfentanyl and 4-Anilinopiperidine, Precursor Chemicals Used in the Illicit Manufacture of Fentanyl, as List I Chemicals, \n 85 FR 20822 (Apr. 15, 2020).\n \n \n \n \n 11 \n  \n <span class=\"match\">Designation</span> of Benzylfentanyl and 4-Anilinopiperidine, Precursor Chemicals Used in the Illicit Manufacture of Fentanyl, as List I Chemicals, \n 85 FR 20822 (Apr. 15, 2020).); See Also \n <span class=\"match\">Designation</span> of Halides of 4-Anilinopiperidine as List 1 Chemicals, \n 88 FR 74352 (Oct. 31, 2023).\n \n \n \n \n 12 \n  \n <span class=\"match\">Designation</span> of 4-Piperidone as a List"},{"title":"Designation of Propionyl Chloride as a List I Chemical","type":"Proposed Rule","abstract":"The Drug Enforcement Administration is proposing the control of propionyl chloride as a list I chemical under the Controlled Substances Act (CSA). The Drug Enforcement Administration finds that propionyl chloride is used in the illicit manufacture of the controlled substances fentanyl, fentanyl analogues and fentanyl-related substances, and is important to the manufacture of these substances. In the respective synthetic pathways in which it is used to manufacture those substances, it is a replacement for propionic anhydride, which is currently a list I chemical. If finalized, the proposed rule would subject handlers of propionyl chloride to the chemical regulatory provisions of the CSA and its implementing regulations. This proposed rulemaking does not establish a threshold for domestic and international transactions of propionyl chloride. As such, all transactions of propionyl chloride, regardless of size, shall be regulated. In addition, chemical mixtures containing propionyl chloride are not exempt from regulatory requirements at any concentration. Therefore, all transactions of chemical mixtures containing any quantity of propionyl chloride shall be regulated pursuant to the CSA. Although no automatic exemption is available, manufacturers may submit an application for exemption.","document_number":"2025-09983","html_url":"https://www.federalregister.gov/documents/2025/06/03/2025-09983/designation-of-propionyl-chloride-as-a-list-i-chemical","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-06-03/pdf/2025-09983.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-09983.pdf?1748868312","publication_date":"2025-06-03","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":"23, 2007).\n \n \n \n \n 9 \n  \n <span class=\"match\">Designation</span> of Benzylfentanyl and 4-Anilinopiperidine, Precursor Chemicals Used in the Illicit Manufacture of Fentanyl, as List I Chemicals, \n 85 FR 20822 (Apr. 15, 2020).\n \n \n \n \n 10 \n  \n <span class=\"match\">Designation</span> of Benzylfentanyl and 4-Anilinopiperidine, Precursor Chemicals Used in the Illicit Manufacture of Fentanyl, as List I Chemicals, \n 85 FR 20822 (Apr. 15, 2020).); See Also \n <span class=\"match\">Designation</span> of Halides of 4-Anilinopiperidine as List 1 Chemicals, \n 88 FR 74352 (Oct. 31, 2023).\n \n \n \n \n 11 \n  \n <span class=\"match\">Designation</span> of 4-Piperidone as a List"},{"title":"Self-Regulatory Organizations; Cboe C2 Exchange, Inc.; Notice of Filing and Immediate Effectiveness of a Proposed Rule Change To Amend Rule 1.1 (Definitions) To Add New Designation “L” to the Definition of “Capacity”","type":"Notice","abstract":null,"document_number":"2026-01206","html_url":"https://www.federalregister.gov/documents/2026/01/23/2026-01206/self-regulatory-organizations-cboe-c2-exchange-inc-notice-of-filing-and-immediate-effectiveness-of-a","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-01-23/pdf/2026-01206.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-01206.pdf?1769089509","publication_date":"2026-01-23","agencies":[{"raw_name":"SECURITIES AND EXCHANGE COMMISSION","name":"Securities and Exchange Commission","id":466,"url":"https://www.federalregister.gov/agencies/securities-and-exchange-commission","json_url":"https://www.federalregister.gov/api/v1/agencies/466","parent_id":null,"slug":"securities-and-exchange-commission"}],"excerpts":"240.19b-4(f)(6).\n \n \n I. Self-Regulatory Organization's Statement of the Terms of Substance of the <span class=\"match\">Proposed</span> Rule Change \n Cboe C2 Exchange, Inc. (“C2” or the “Exchange”) is filing with the Securities and Exchange Commission (“Commission” or “SEC”) a <span class=\"match\">proposed</span> rule change to amend Rule 1.1 (Definitions) to add new <span class=\"match\">designation</span> “L” to the definition of “Capacity”. The text of the <span class=\"match\">proposed</span> rule change is provided in Exhibit 5. \n \n The text of the <span class=\"match\">proposed</span> rule change is also available on the Commission's website (\n https://www.sec.gov/rules/sro.shtml "}]}