{"description":"Documents matching 'provide information demonstrating they have'","count":10000,"total_pages":50,"next_page_url":"https://www.federalregister.gov/api/v1/documents?conditions%5Bterm%5D=provide+information+demonstrating+they+have&format=json&page=2","results":[{"title":"Protein Efficiency Ratio Rat Bioassay Studies To Demonstrate That a New Infant Formula Supports the Quality Factor of Sufficient Biological Quality of Protein; Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA or we) is announcing the availability of a guidance entitled \"Protein Efficiency Ratio (PER) Rat Bioassay Studies to Demonstrate That a New Infant Formula Supports the Quality Factor of Sufficient Biological Quality of Protein.\" The guidance provides information for manufacturers and contract laboratories that perform PER studies to assist in designing, conducting, evaluating, and reporting PER studies. The guidance explains \"appropriate modifications\" of AOAC Official Method 960.48 (the AOAC Method) with the aim of supporting industry in successfully conducting PER studies that demonstrate that a new infant formula meets the quality factor of sufficient biological quality of protein when fed as the sole source of nutrition. The guidance finalizes the approach presented in the draft guidance issued in 2023.","document_number":"2026-10284","html_url":"https://www.federalregister.gov/documents/2026/05/22/2026-10284/protein-efficiency-ratio-rat-bioassay-studies-to-demonstrate-that-a-new-infant-formula-supports-the","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-05-22/pdf/2026-10284.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-10284.pdf?1779367512","publication_date":"2026-05-22","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":"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":"comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else's Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on \n https://www.regulations.gov. \n \n • If you want to submit a comment with confidential information that you do not wish to be made available"},{"title":"Demonstrating Substantial Evidence of Effectiveness for Human Drug and Biological Products; Revised Draft Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a revised draft guidance for industry titled \"Demonstrating Substantial Evidence of Effectiveness for Human Drug and Biological Products.\" FDA has revised and is reissuing this draft guidance in response to public comments and to changes in drug development by focusing on generating rigorous scientific evidence in the most efficient manner. Advances in our understanding of biological processes and the increasing availability of high-quality data have transformed the evidentiary landscape for drug development. Given these advances, the draft guidance discusses the many factors that can impact the strength of evidence of effectiveness for a drug and clarifies how sponsors can rely on one adequate and well-controlled clinical investigation with confirmatory evidence to satisfy the substantial evidence of effectiveness standard. When final, this guidance will replace the 1998 guidance titled \"Providing Clinical Evidence of Effectiveness for Human Drug and Biological Products.\"","document_number":"2026-12622","html_url":"https://www.federalregister.gov/documents/2026/06/24/2026-12622/demonstrating-substantial-evidence-of-effectiveness-for-human-drug-and-biological-products-revised","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-24/pdf/2026-12622.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-12622.pdf?1782141309","publication_date":"2026-06-24","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":"comment does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else's Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on \n https://www.regulations.gov. \n \n • If you want to submit a comment with confidential information that you do not wish to be made available"},{"title":"Scientific Considerations in Demonstrating Biosimilarity to a Reference Product: Updated Recommendations for Assessing the Need for Comparative Efficacy Studies; Draft Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a draft guidance for industry entitled \"Scientific Considerations in Demonstrating Biosimilarity to a Reference Product: Updated Recommendations for Assessing the Need for Comparative Efficacy Studies.\" This draft guidance describes considerations regarding a comparative clinical study or studies with efficacy endpoints (a comparative efficacy study or CES) intended to support a demonstration that a proposed therapeutic protein product is biosimilar to a reference product for the purpose of submitting a marketing application under the Public Health Service Act (PHS Act).","document_number":"2025-20380","html_url":"https://www.federalregister.gov/documents/2025/11/20/2025-20380/scientific-considerations-in-demonstrating-biosimilarity-to-a-reference-product-updated","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-11-20/pdf/2025-20380.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-20380.pdf?1763559916","publication_date":"2025-11-20","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":"does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else's Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on \n https://www.regulations.gov \n .\n \n • If you want to submit a comment with confidential information that you do not wish to be made available"},{"title":"Agency Information Collection Activities; Suspensions Pending Appeal and Bonding","type":"Notice","abstract":"In accordance with the Paperwork Reduction Act of 1995 (PRA), ONRR is proposing to renew an information collection. Through this Information Collection Request renewal (ICR), ONRR seeks renewed authority to collect information related to the paperwork requirements necessary to post a surety or bond or demonstrate financial solvency.","document_number":"2026-07750","html_url":"https://www.federalregister.gov/documents/2026/04/21/2026-07750/agency-information-collection-activities-suspensions-pending-appeal-and-bonding","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-04-21/pdf/2026-07750.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-07750.pdf?1776689115","publication_date":"2026-04-21","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":"Office of Natural Resources Revenue","name":"Natural Resources Revenue Office","id":586,"url":"https://www.federalregister.gov/agencies/natural-resources-revenue-office","json_url":"https://www.federalregister.gov/api/v1/agencies/586","parent_id":253,"slug":"natural-resources-revenue-office"}],"excerpts":"8(d)(1). This helps ONRR to assess the impact of its information collection requirements and minimize the public's reporting burden. It also helps the public understand ONRR's information collection requirements and provide the requested data in the desired format. \n ONRR is especially interested in public comments addressing the following: \n (1) Whether the collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; \n (2) The accuracy of ONRR's estimate"},{"title":"Considerations in Demonstrating Interchangeability With a Reference Product: Update; Draft Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a draft guidance for industry entitled \"Considerations in Demonstrating Interchangeability With a Reference Product: Update.\" This draft guidance describes considerations regarding a switching study or studies intended to support a demonstration that a proposed therapeutic protein product is interchangeable with a reference product for the purposes of submitting a marketing application or supplement under the Public Health Service Act (PHS Act). After considering any comments received in the docket for this draft guidance, we intend to revise the final guidance for industry entitled \"Considerations in Demonstrating Interchangeability With a Reference Product\" issued on May 14, 2019, to amend sections in that document regarding the subject addressed in this draft guidance.","document_number":"2024-13429","html_url":"https://www.federalregister.gov/documents/2024/06/21/2024-13429/considerations-in-demonstrating-interchangeability-with-a-reference-product-update-draft-guidance","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-06-21/pdf/2024-13429.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-13429.pdf?1718887516","publication_date":"2024-06-21","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":"does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else's Social Security number, or confidential business information, such \n \n as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on \n https://www.regulations.gov. \n \n • If you want to submit a comment with confidential information that you do not wish to be made available"},{"title":"Demonstrating Bioequivalence for Type A Medicated Articles Containing Active Pharmaceutical Ingredient(s) Considered To Be Poorly Soluble in Aqueous Media, That Exhibit Little to No Systemic Bioavailability, and Are Locally Acting; Guidance for Industry; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance for industry (GFI) #279 entitled \"Demonstrating Bioequivalence for Type A Medicated Articles Containing Active Pharmaceutical Ingredient(s) Considered to be Poorly Soluble in Aqueous Media, That Exhibit Little to No Systemic Bioavailability, and Are Locally Acting.\" This final guidance describes an approach to satisfy the requirements for the completion of the Bioequivalence technical section for generic Type A medicated articles (TAMAs) containing poorly soluble, locally acting, active pharmaceutical ingredients (APIs) that have little to no systemic absorption, and for which blood level studies are not considered appropriate to demonstrate product bioequivalence. The suggested approach described in this guidance uses a combination of in vitro and in vivo data to support a determination of bioequivalence to address the unique challenges associated with demonstrating bioequivalence of TAMAs containing poorly soluble, locally acting APIs that have little to no systemic absorption.","document_number":"2024-13690","html_url":"https://www.federalregister.gov/documents/2024/06/21/2024-13690/demonstrating-bioequivalence-for-type-a-medicated-articles-containing-active-pharmaceutical","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-06-21/pdf/2024-13690.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-13690.pdf?1718887546","publication_date":"2024-06-21","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":"does not include any confidential information that you or a third party may not wish to be posted, such as medical information, your or anyone else's Social Security number, or confidential business information, such as a manufacturing process. Please note that if you include your name, contact information, or other information that identifies you in the body of your comments, that information will be posted on \n https://www.regulations.gov \n .\n \n • If you want to submit a comment with confidential information that you do not wish to be made available"},{"title":"Requirement To Provide Paper Statements in Certain Cases-Amendments to Electronic Disclosure Safe Harbors","type":"Proposed Rule","abstract":"The Department of Labor (Department) is proposing narrow amendments to two separate electronic disclosure safe harbors for purposes of implementing section 338 of the SECURE 2.0 Act of 2022 (SECURE 2.0). Taken together, the two existing safe harbors permit the broad use of electronic disclosure under prescribed conditions for the furnishing of required disclosures under Title I of the Employee Retirement Income Security Act of 1974 (ERISA). Section 338 of SECURE 2.0 amended section 105(a)(2) of ERISA to require retirement plans to provide paper benefit statements in certain cases. Section 338 also instructed the Department to update its electronic disclosure safe harbors in connection with the statutory changes. The proposed amendments would implement these Congressional mandates.","document_number":"2026-03723","html_url":"https://www.federalregister.gov/documents/2026/02/25/2026-03723/requirement-to-provide-paper-statements-in-certain-cases-amendments-to-electronic-disclosure-safe","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-02-25/pdf/2026-03723.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-03723.pdf?1771940709","publication_date":"2026-02-25","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":"Employee Benefits Security Administration","name":"Employee Benefits Security Administration","id":131,"url":"https://www.federalregister.gov/agencies/employee-benefits-security-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/131","parent_id":271,"slug":"employee-benefits-security-administration"}],"excerpts":"comments that: \n • Evaluate whether the collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility \n • Evaluate the accuracy of the agency's estimate of the burden of the collection of information, including the validity of the methodology and assumptions used, \n • Enhance the quality, utility, and clarity of the information to be collected, and \n \n • Minimize the burden of the collection of information on those who are to respond, including through the"},{"title":"Public Notice: Design Challenge for National Memorial to Fallen Highway Workers in Work Zones","type":"Notice","abstract":"FHWA invites detailed proposals for the design, construction, and installation of a National Fallen Highway Workers Memorial. Proposals should demonstrate both a compelling design vision and a feasible approach to implementation. This memorial will honor the American workers who have lost their lives in highway work zones and serve as a national symbol of the ongoing commitment to work zone safety.","document_number":"2026-12440","html_url":"https://www.federalregister.gov/documents/2026/06/22/2026-12440/public-notice-design-challenge-for-national-memorial-to-fallen-highway-workers-in-work-zones","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-22/pdf/2026-12440.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-12440.pdf?1781786719","publication_date":"2026-06-22","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 Highway Administration","name":"Federal Highway Administration","id":170,"url":"https://www.federalregister.gov/agencies/federal-highway-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/170","parent_id":492,"slug":"federal-highway-administration"}],"excerpts":"National Fallen Highway Workers Memorial. Proposals should demonstrate both a compelling design vision and a feasible approach to implementation. This memorial will honor the American workers who have lost their lives in highway work zones and serve as a national symbol of the ongoing commitment to work zone safety. \n \n \n DATES: \n Submissions must be received on or before October 20, 2026. \n \n \n ADDRESSES: \n \n Submissions should be emailed to: \n WZMemorial@dot.gov. \n \n \n \n FOR FURTHER INFORMATION CONTACT: \n \n For questions about this notice, please contact"},{"title":"Agency Information Collection Activities: Proposed Collection; Comment Request-The Special Supplemental Nutrition Program for Women, Infants and Children (WIC) Breastfeeding Award of Excellence","type":"Notice","abstract":"In accordance with the Paperwork Reduction Act of 1995, this notice invites the general public and other public agencies to comment on this proposed information collection. This collection is a revision of a currently approved collection for awarding local agencies for excellence in WIC breastfeeding services and support. The Child Nutrition Act of 1966 at 42 U.S. Code Sec. 1786(h)(4)(B), requires that the Department of Agriculture (USDA) establish a program to recognize WIC local agencies and clinics that demonstrate exemplary breastfeeding promotion and support activities.","document_number":"2026-04773","html_url":"https://www.federalregister.gov/documents/2026/03/11/2026-04773/agency-information-collection-activities-proposed-collection-comment-request-the-special","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-03-11/pdf/2026-04773.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-04773.pdf?1773146716","publication_date":"2026-03-11","agencies":[{"raw_name":"DEPARTMENT OF AGRICULTURE","name":"Agriculture Department","id":12,"url":"https://www.federalregister.gov/agencies/agriculture-department","json_url":"https://www.federalregister.gov/api/v1/agencies/12","parent_id":null,"slug":"agriculture-department"},{"raw_name":"Food and Nutrition Service","name":"Food and Nutrition Service","id":200,"url":"https://www.federalregister.gov/agencies/food-and-nutrition-service","json_url":"https://www.federalregister.gov/api/v1/agencies/200","parent_id":12,"slug":"food-and-nutrition-service"}],"excerpts":"the information shall have practical utility; (b) the accuracy of the agency's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions that were used; (c) ways to enhance the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on those who are to respond, including use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology"},{"title":"21st Century Cures Act: Establishment of Disincentives for Health Care Providers That Have Committed Information Blocking","type":"Rule","abstract":"This final rule implements the provision of the 21st Century Cures Act specifying that a health care provider determined by the HHS Inspector General to have committed information blocking shall be referred to the appropriate agency to be subject to appropriate disincentives set forth through notice and comment rulemaking. This rulemaking establishes, for certain health care providers, a set of appropriate disincentives using authorities under applicable Federal law.","document_number":"2024-13793","html_url":"https://www.federalregister.gov/documents/2024/07/01/2024-13793/21st-century-cures-act-establishment-of-disincentives-for-health-care-providers-that-have-committed","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-07-01/pdf/2024-13793.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-13793.pdf?1719432919","publication_date":"2024-07-01","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"},{"raw_name":"Office of the Secretary"}],"excerpts":"an appropriate agency. The Disincentives Proposed Rule further proposed to publicly post information on ONC's website about health care providers that have been determined by OIG to have committed information blocking and subsequently referred by OIG to an appropriate agency to be subject to appropriate disincentives, as well about health IT developers of certified health \n \n IT and HIEs/HINs and that have been determined by OIG to have committed information blocking. Finally, the Disincentives Proposed Rule requested public comment on establishing"},{"title":"Improving SBA Disaster Loan Ability To Provide Meaningful and Timely Assistance","type":"Rule","abstract":"The U.S. Small Business Administration (SBA or Agency) is issuing this interim final rule (IFR) to ensure the timely and effective delivery of assistance under the Disaster Loan Program authorized under section 7(b) of the Small Business Act (15 U.S.C. 636(b)) (\"Disaster Loan Program\") following a Presidentially declared disaster. This rule preempts certain state and local requirements impacting the repair, rehabilitation, or replacement of damaged or destroyed property and associated activities financed by the Disaster Loan Program when such requirements cause delay in the use of SBA Disaster Loan Program proceeds. The rule is necessary to reconcile non- federal requirements that undermine Congress's objective of rapid housing and business recovery, public health and safety restoration, and economic stabilization after disasters.","document_number":"2026-01797","html_url":"https://www.federalregister.gov/documents/2026/01/29/2026-01797/improving-sba-disaster-loan-ability-to-provide-meaningful-and-timely-assistance","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-01-29/pdf/2026-01797.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-01797.pdf?1769607917","publication_date":"2026-01-29","agencies":[{"raw_name":"SMALL BUSINESS ADMINISTRATION","name":"Small Business Administration","id":468,"url":"https://www.federalregister.gov/agencies/small-business-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/468","parent_id":null,"slug":"small-business-administration"}],"excerpts":"Regulatory Information Number (RIN) for this \n \n rulemaking. All comments received will be posted on \n http://www.regulations.gov. \n If you wish to submit confidential business information (CBI) as defined in the User Notice at \n http://www.regulations.gov, \n please submit the comments to Laura Maas and highlight the information that you consider to be CBI and explain why you believe this information should be held confidential. SBA will make a final determination as to whether the comments will be published or not.\n \n \n \n FOR FURTHER INFORMATION CONTACT:"},{"title":"Gross Proceeds Reporting by Brokers That Regularly Provide Services Effectuating Digital Asset Sales","type":"Rule","abstract":"This document contains final regulations regarding information reporting by brokers that regularly provide services effectuating certain digital asset sales and exchanges. The final regulations require these brokers to file information returns and furnish payee statements reporting gross proceeds on dispositions of digital assets effected for customers in certain sale or exchange transactions.","document_number":"2024-30496","html_url":"https://www.federalregister.gov/documents/2024/12/30/2024-30496/gross-proceeds-reporting-by-brokers-that-regularly-provide-services-effectuating-digital-asset-sales","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-12-30/pdf/2024-30496.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-30496.pdf?1735307119","publication_date":"2024-12-30","agencies":[{"raw_name":"DEPARTMENT OF THE TREASURY","name":"Treasury Department","id":497,"url":"https://www.federalregister.gov/agencies/treasury-department","json_url":"https://www.federalregister.gov/api/v1/agencies/497","parent_id":null,"slug":"treasury-department"},{"raw_name":"Internal Revenue Service","name":"Internal Revenue Service","id":254,"url":"https://www.federalregister.gov/agencies/internal-revenue-service","json_url":"https://www.federalregister.gov/api/v1/agencies/254","parent_id":497,"slug":"internal-revenue-service"}],"excerpts":"Additional Information Reporting and Clarified Guidance Could Improve Tax Compliance, \n 28, GAO-20-188 (Washington, DC: February 2020). Reducing the tax gap and providing information to taxpayers is no less important when a DeFi participant, acting as a middleman, provides parties with technological services that enable those parties to carry out the DeFi transaction. Indeed, clear information reporting rules that require reporting of gross proceeds from a sale of digital assets in DeFi transactions will help the IRS identify taxpayers who have engaged"},{"title":"Implementing the Freedom of Information Act and Privacy Act","type":"Proposed Rule","abstract":"The Office of the National Cyber Director (ONCD) is issuing its first Freedom of Information Act (FOIA) and Privacy Act regulations. These regulations reflect ONCD's process for responding to requests for information and affirm its commitment to provide the fullest possible disclosure of records to the public.","document_number":"2026-06195","html_url":"https://www.federalregister.gov/documents/2026/03/31/2026-06195/implementing-the-freedom-of-information-act-and-privacy-act","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-03-31/pdf/2026-06195.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-06195.pdf?1774874716","publication_date":"2026-03-31","agencies":[{"raw_name":"Office of the National Cyber Director","name":"Office of the National Cyber Director","id":613,"url":"https://www.federalregister.gov/agencies/office-of-the-national-cyber-director","json_url":"https://www.federalregister.gov/api/v1/agencies/613","parent_id":538,"slug":"office-of-the-national-cyber-director"}],"excerpts":"unless the submitter requests, and provides justification for, a longer designation period.\n \n \n (d) \n Notice to submitters. \n ONCD shall provide a submitter with prompt written notice of a FOIA request or administrative appeal that seeks its business information to give the submitter an opportunity to object to disclosure of any specified portion of that information. The notice shall either describe the business information requested or include copies of the requested records or record portions containing the information. When notification of a voluminous"},{"title":"Scaling Critical Suppliers in Domestic Supply Chains","type":"Notice","abstract":"The U.S. Small Business Administration (SBA) requests public input to inform the design of near-term initiatives intended to strengthen domestic manufacturing capacity for critical components, subcomponents, materials, tooling, and specialized capabilities essential to economic resilience and national security. This request focuses on identifying opportunities to rapidly scale existing domestic supplier capacity in areas characterized by supply chain constraints or choke points. SBA is particularly interested in gaps where qualifying domestic small businesses have a demonstrated operating history but are unable to reach a specific near-term milestone due to a capital shortfall. Information received in response to this Request for information (RFI) will inform the development of SBA innovation programs and initiatives, including potential prize competitions designed to deliver measurable increases in production capacity, supplier participation, and supply chain resilience within a compressed execution window.","document_number":"2026-08554","html_url":"https://www.federalregister.gov/documents/2026/05/01/2026-08554/scaling-critical-suppliers-in-domestic-supply-chains","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-05-01/pdf/2026-08554.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-08554.pdf?1777553125","publication_date":"2026-05-01","agencies":[{"raw_name":"SMALL BUSINESS ADMINISTRATION","name":"Small Business Administration","id":468,"url":"https://www.federalregister.gov/agencies/small-business-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/468","parent_id":null,"slug":"small-business-administration"}],"excerpts":"particularly interested in gaps where qualifying domestic small businesses have a demonstrated operating history but are unable to reach a specific near-term milestone due to a capital shortfall. Information received in response to this Request for information (RFI) will inform the development of SBA innovation programs and initiatives, including potential prize competitions designed to deliver measurable increases in production capacity, supplier participation, and supply chain resilience within a compressed execution window. \n \n \n DATES: \n Submit comments"},{"title":"Commercial Driver's License: Massachusetts Department of State Police; Application for Exemption","type":"Notice","abstract":"FMCSA requests public comment on the Massachusetts Department of State Police's request for an exemption to conduct modified commercial driver's license (CDL) skills test exams on the island of Martha's Vineyard. According to the applicant, the island of Martha's Vineyard does not have the infrastructure for applicant drivers to demonstrate the two sets of lane changes required by the CDL skills test.","document_number":"2025-12202","html_url":"https://www.federalregister.gov/documents/2025/07/01/2025-12202/commercial-drivers-license-massachusetts-department-of-state-police-application-for-exemption","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-07-01/pdf/2025-12202.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-12202.pdf?1751287522","publication_date":"2025-07-01","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 Motor Carrier Safety Administration","name":"Federal Motor Carrier Safety Administration","id":181,"url":"https://www.federalregister.gov/agencies/federal-motor-carrier-safety-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/181","parent_id":492,"slug":"federal-motor-carrier-safety-administration"}],"excerpts":"closing date will be filed in the public docket and will be considered to the extent practicable. \n B. Confidential Business Information (CBI) \n \n CBI is commercial or financial information that is both customarily and actually treated as private by its owner. Under the Freedom of Information Act (5 U.S.C. 552), CBI is exempt from public disclosure. If your comments responsive to the notice contain commercial or financial information that is customarily treated as private, that you actually treat as private, and that is relevant or responsive to the notice"},{"title":"Agency Information Collection Activities; Request for Public Comment","type":"Notice","abstract":"The Department of Labor (the Department), in accordance with the Paperwork Reduction Act, provides the general public and Federal agencies with an opportunity to comment on proposed and continuing collections of information. This helps the Department assess the impact of its information collection requirements and minimize the public's reporting burden. It also helps the public understand the Department's information collection requirements and provide the requested data in the desired format. The Employee Benefits Security Administration (EBSA) is soliciting comments on the proposed extension of the information collection requests (ICRs) contained in the documents described below. A copy of the ICRs may be obtained by contacting the office listed in the ADDRESSES section of this notice. ICRs also are available at reginfo.gov (http://www.reginfo.gov/public/do/PRAMain).","document_number":"2026-03145","html_url":"https://www.federalregister.gov/documents/2026/02/18/2026-03145/agency-information-collection-activities-request-for-public-comment","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-02-18/pdf/2026-03145.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-03145.pdf?1771335919","publication_date":"2026-02-18","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"}],"excerpts":"Reduction Act, provides the general public and Federal agencies with an opportunity to comment on proposed and continuing collections of information. This helps the Department assess the impact of its information collection requirements and minimize the public's reporting burden. It also helps the public understand the Department's information collection requirements and provide the requested data in the desired format. The Employee Benefits Security Administration (EBSA) is soliciting comments on the proposed extension of the information collection"},{"title":"Personnel Development To Improve Services and Results for Children With Disabilities-Interdisciplinary Preparation of Early Intervention, Special Education, and Related Services Personnel Serving Children With Disabilities Who Have High-Intensity Needs","type":"Notice","abstract":"The Department of Education (Department) is issuing a notice inviting applications for new awards for fiscal year (FY) 2025 for Personnel Development to Improve Services and Results for Children with Disabilities--Interdisciplinary Preparation of Early Intervention, Special Education, and Related Services Personnel Serving Children with Disabilities who have High-Intensity Needs.","document_number":"2025-09431","html_url":"https://www.federalregister.gov/documents/2025/05/27/2025-09431/personnel-development-to-improve-services-and-results-for-children-with","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-05-27/pdf/2025-09431.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-09431.pdf?1748004317","publication_date":"2025-05-27","agencies":[{"raw_name":"DEPARTMENT OF EDUCATION","name":"Education Department","id":126,"url":"https://www.federalregister.gov/agencies/education-department","json_url":"https://www.federalregister.gov/api/v1/agencies/126","parent_id":null,"slug":"education-department"}],"excerpts":"Related Services Personnel Serving Children with Disabilities who have High-Intensity Needs. \n \n \n DATES: \n \n \n Applications Available: \n May 27, 2025.\n \n \n Deadline for Transmittal of Applications: \n June 26, 2025.\n \n \n Deadline for Intergovernmental Review: \n August 25, 2025.\n \n \n Pre-Application Webinar Information: \n No later than June 2, 2025, the Office of Special Education and Rehabilitative Services will post details on pre-recorded informational webinars designed to provide technical assistance to interested applicants. Links to the webinars"},{"title":"Federal Site Providing Ground Safety Services and Oversight for Launch or Reentry Activities Conducted From a Commercial Site Located on Land Owned by a Federal Site","type":"Notice","abstract":"This document clarifies that, in instances where launch or reentry activities are conducted from an FAA-licensed commercial site located on land that is owned by a Federal site that the commercial site uses pursuant to an agreement with the Federal site, and the Federal site provides ground safety services and oversight, the vehicle operator may be able to demonstrate an equivalent level of safety to the FAA's ground safety requirements.","document_number":"2025-08097","html_url":"https://www.federalregister.gov/documents/2025/05/09/2025-08097/federal-site-providing-ground-safety-services-and-oversight-for-launch-or-reentry-activities","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-05-09/pdf/2025-08097.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2025-08097.pdf?1746708312","publication_date":"2025-05-09","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":"with the Federal site, and the Federal site provides ground safety services and oversight, the vehicle operator may be able to demonstrate an equivalent level of safety to the FAA's ground safety requirements. \n \n \n FOR FURTHER INFORMATION CONTACT: \n \n For additional information concerning this action, contact Katie Cranor, Acting Executive Director, Office of Operational Safety, 800 Independence Ave. SW, Washington, DC 20591; (202) 267-9525; \n 9-AST-Inquiries@faa.gov. \n \n \n \n \n SUPPLEMENTARY INFORMATION: \n I. Authority \n \n The Commercial Space Launch"},{"title":"Information Collection Being Reviewed by the Federal Communications Commission Under Delegated Authority","type":"Notice","abstract":"As part of its continuing effort to reduce paperwork burdens, and as required by the Paperwork Reduction Act (PRA) of 1995, the Federal Communications Commission (FCC or Commission) invites the general public and other Federal agencies to take this opportunity to comment on the following information collections. Comments are requested concerning: whether the proposed collection of information is necessary for the proper performance of the functions of the Commission, including whether the information shall have practical utility; the accuracy of the Commission's burden estimate; ways to enhance the quality, utility, and clarity of the information collected; ways to minimize the burden of the collection of information on the respondents, including the use of automated collection burden on small business concerns with fewer than 25 employees. The FCC may not conduct or sponsor a collection of information unless it displays a currently valid OMB control number. No person shall be subject to any penalty for failing to comply with a collection of information subject to the PRA that does not display a valid OMB control number.","document_number":"2026-01557","html_url":"https://www.federalregister.gov/documents/2026/01/27/2026-01557/information-collection-being-reviewed-by-the-federal-communications-commission-under-delegated","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-01-27/pdf/2026-01557.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-01557.pdf?1769435120","publication_date":"2026-01-27","agencies":[{"raw_name":"FEDERAL COMMUNICATIONS COMMISSION","name":"Federal Communications Commission","id":161,"url":"https://www.federalregister.gov/agencies/federal-communications-commission","json_url":"https://www.federalregister.gov/api/v1/agencies/161","parent_id":null,"slug":"federal-communications-commission"}],"excerpts":"agencies to take this opportunity to comment on the following information collections. Comments are requested concerning: whether the proposed collection of information is necessary for the proper performance of the functions of the Commission, including whether the information shall have practical utility; the accuracy of the Commission's burden estimate; ways to enhance the quality, utility, and clarity of the information collected; ways to minimize the burden of the collection of information on the respondents, including the use of automated collection"},{"title":"Information Collections Being Reviewed by the Federal Communications Commission Under Delegated Authority","type":"Notice","abstract":"As part of its continuing effort to reduce paperwork burdens, and as required by the Paperwork Reduction Act (PRA) of 1995, the Federal Communications Commission (FCC or the Commission) invites the general public and other Federal agencies to take this opportunity to comment on the following information collection. Comments are requested concerning: whether the proposed collection of information is necessary for the proper performance of the functions of the Commission, including whether the information shall have practical utility; the accuracy of the Commission's burden estimate; ways to enhance the quality, utility, and clarity of the information collected; ways to minimize the burden of the collection of information on the respondents, including the use of automated collection techniques or other forms of information technology; and ways to further reduce the information collection burden on small business concerns with fewer than 25 employees. The FCC may not conduct or sponsor a collection of information unless it displays a currently valid control number. No person shall be subject to any penalty for failing to comply with a collection of information subject to the PRA that does not display a valid Office of Management and Budget (OMB) control number.","document_number":"2026-07068","html_url":"https://www.federalregister.gov/documents/2026/04/13/2026-07068/information-collections-being-reviewed-by-the-federal-communications-commission-under-delegated","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-04-13/pdf/2026-07068.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-07068.pdf?1775825114","publication_date":"2026-04-13","agencies":[{"raw_name":"FEDERAL COMMUNICATIONS COMMISSION","name":"Federal Communications Commission","id":161,"url":"https://www.federalregister.gov/agencies/federal-communications-commission","json_url":"https://www.federalregister.gov/api/v1/agencies/161","parent_id":null,"slug":"federal-communications-commission"}],"excerpts":"following information collection. Comments are requested concerning: whether the proposed collection of information is necessary for the proper performance of the functions of the Commission, including whether the information shall have practical utility; the accuracy of the Commission's burden estimate; ways to enhance the quality, utility, and clarity of the information collected; ways to minimize the burden of the collection of information on the respondents, including the use of automated collection techniques or other forms of information technology;"}]}