Airworthiness Directives; The Boeing Company Airplanes
The FAA proposes to supersede Airworthiness Directive 2024-01-01 for certain The Boeing Company Model 787-8, 787-9, and 787-10 airplanes to address an unsafe condition.
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Vadescana Double-Stranded RNA; Exemption From the Requirement of a Tolerance
The US Environmental Protection Agency (EPA) has established an exemption for residues of Vadescana double-stranded RNA in honey and honeycomb when used according to the label and good agricultural practices, eliminating the need for a maximum permissible level.
EPA Corrects Cancellation Order for Chlorpyrifos
The Environmental Protection Agency (EPA) is correcting a cancellation order for chlorpyrifos, specifically rescinding the termination of asparagus use in Michigan for Pilot 4E Chlorpyrifos Agricultural Insecticide.
NRC Submits Proposed Collection of Information for Visitor Access Request System (VARS)
The U.S. Nuclear Regulatory Commission (NRC) has submitted a proposed collection of information to the Office of Management and Budget (OMB) for review, related to the Visitor Access Request System (VARS).
US Nuclear Regulatory Commission Holds 727th Meeting of Advisory Committee on Reactor Safeguards (ACRS)
The 727th Meeting of the Advisory Committee on Reactor Safeguards (ACRS) took place, focusing on reactor safety issues. The committee, established by the U.S. Nuclear Regulatory Commission, aims to provide recommendations for improving reactor safety.
IWG Meetings Scheduled for WRC-27 Advisory Committee
Informal Working Groups 1-4 of the WRC-27 Advisory Committee have scheduled public meetings for the 2027 World Radiocommunication Conference. The meetings' dates and times have not been specified.
FCC Publishes Correction to Petition for Reconsideration of Rulemaking Proceeding
The Federal Communications Commission (FCC) published a correction to its May 30, 2025, document regarding Petitions for Reconsideration, correcting an incorrect date for filing replies to oppositions.
FCC Proposes Non-IP Caller ID Authentication Frameworks
The Federal Communications Commission proposes requiring providers to implement non-IP caller ID authentication frameworks, aligning with the TRACED Act requirements.
Federal Communications Commission Reviews FY 2025 Regulatory Fees
The Federal Communications Commission is seeking public comment on revising the fee schedule for FY 2025 and addressing several additional regulatory fee issues.
Submission for OMB Review; Termination Settlement Proposal Forms (SFs 1435-1440)
The Regulatory Secretariat Division has submitted to OMB a request to review and approve an extension of a previously approved information collection requirement for termination settlement proposal forms (SF 1435-1440) under the Paperwork Reduction Act.
Submission for OMB Review; Indirect Cost Rate Proposals, Payments to Small Business Subcontractors, and Bankruptcy Notifications
The Regulatory Secretariat Division has submitted to OMB a request to review and approve an extension of an approved information collection requirement related to indirect cost rate proposals, payments to small business subcontractors, and bankruptcy notifications under the Paperwork Reduction Act.
Submission for OMB Review; Federal Acquisition Regulation Part 46 Requirements
The Regulatory Secretariat Division has submitted to OMB a request to review and approve an extension of a previously approved information collection requirement regarding Federal Acquisition Regulation part 46 requirements, as mandated by the Paperwork Reduction Act.
Submission for OMB Review; Federal Acquisition Regulation Part 7 Requirements
The Regulatory Secretariat Division has submitted to OMB a request to review and approve an extension of a previously approved information collection requirement regarding Federal Acquisition Regulation part 7 requirements, as mandated by the Paperwork Reduction Act.
Submission for OMB Review; Cost Accounting Standards Administration
The Regulatory Secretariat Division has submitted to OMB a request to review and approve an extension of a previously approved information collection requirement regarding cost accounting standards administration, as mandated by the Paperwork Reduction Act.
USTR Requests Comments on Caribbean Basin Initiative Report
The USTR is seeking public comments on the Caribbean Basin Initiative's performance and eligibility for benefits by December 31, 2025, to inform its report to Congress.
FDA Announces Public Advisory Committee Meeting for Belantamab Mafodotin BLA 761440
The FDA is hosting a public meeting of the Oncologic Drugs Advisory Committee to discuss the biologic license application for Belantamab Mafodotin, and is seeking public comments on the matter.
FDA Announces Collection of Information for New Animal Drug and Veterinary Master Files
The FDA has submitted a proposed collection of information to the Office of Management and Budget for review and clearance, as required by the Paperwork Reduction Act of 1995.
FDA Announces Public Comment Period for Medical Device Accessory Classification Requests
The FDA is seeking public comment on its proposed collection of information related to medical device accessory classification requests, as required by the Paperwork Reduction Act of 1995.
Agency Information Collection Activities; Proposed Collection; Comment Request; Export of Medical Devices; Foreign Letters of Approval
The FDA is seeking public comment on proposed reporting requirements for firms exporting unapproved medical devices, as mandated by the Paperwork Reduction Act of 1995.
FDA Announces Public Comment Period for Manufactured Food Regulatory Program Standards
The Food and Drug Administration is seeking public comment on its proposed collection of information related to its Manufactured Food Regulatory Program Standards under the Paperwork Reduction Act of 1995.
FDA Releases Final Guidance on Pre-Submission Facility Correspondence for Prioritized Generic Drug Submissions
The FDA has announced the availability of a final guidance for industry on pre-submission facility correspondence related to prioritized generic drug submissions, which outlines the facility information to be submitted and how the FDA will use it to set review goals for priority ANDAs.
FDA to Host Public Meeting on Use of Unapproved Fluoride Prescription Drugs in Children
The FDA is hosting a public meeting to gather public input on the use of unapproved prescription drugs containing fluoride in children, and is establishing a public docket for comments on the topic.
FDA Determines Regulatory Review Period for BRIUMVI Patent Extension
The US Food and Drug Administration (FDA) has determined the regulatory review period for BRIUMVI, a human biological product, following patent extension applications submitted to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for POMBILITI Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for POMBILITI, a human biological product, in response to a patent extension application submitted to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for IMPELLA RP FLEX WITH SMART ASSIST
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for the patent extension of IMPELLA RP FLEX WITH SMART ASSIST, a medical device, following submissions to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for AVEIR VR Leadless System
The US Food and Drug Administration (FDA) has determined the regulatory review period for the AVEIR VR Leadless System, a medical device, following patent extension applications submitted to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for XOLREMDI Patent Extension
The FDA has determined the regulatory review period for XOLREMDI, a human drug product, following submissions to the USPTO for patent extension, as required by law.
FDA Determines Regulatory Review Period for VOYDEYA Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for VOYDEYA, a human drug product, in response to a patent extension application submitted to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for VAFSEO Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for VAFSEO, a patent extension application submitted to the US Patent and Trademark Office (USPTO) for a human drug product patent.
FDA Determines Regulatory Review Period for NAVITOR TRANSCATHETER AORTIC VALVE IMPLANT
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for patent extension of the NAVITOR TRANSCATHETER AORTIC VALVE IMPLANT, following submissions to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for ZEVTERA Patent Extension
The US Food and Drug Administration (FDA) has determined the regulatory review period for ZEVTERA, a human drug product, following a patent extension application submitted to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for VOWST Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for VOWST, a human biological product, in response to patent extension applications submitted to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for RIVFLOZA Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for RIVFLOZA, a human drug product, following a patent extension application submitted to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for ROLVEDON Patent Extension
The FDA has published a notice determining the regulatory review period for ROLVEDON, a human biological product, following a patent extension application submitted to the USPTO.
FDA Determines Regulatory Review Period for BEYFORTUS Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for the extension of a patent for a human biological product, submitted by the US Patent and Trademark Office (USPTO).
FHFA Proposes to Rescind System of Records Notice
The Federal Housing Finance Agency (FHFA) is proposing to rescind a System of Records Notice (SORN) related to its Applicant Tracking System (FHFA-25), which was decommissioned and no longer maintained by the Agency.
Federal Court Vacates APHIS Genetically Engineered Organism Rule
A US Federal court has overturned the Animal and Plant Health Inspection Service's (APHIS) May 2020 final rule on genetically modified organisms, restoring the pre-May 2020 regulations and requiring APHIS to revise its regulations to conform to the court's decision, effective December 2, 2024.
US Government Invites Public Comment on Proposed Changes to SNAP Information Collection
The US government is seeking public feedback on a proposed revision to the Supplemental Nutrition Assistance Program (SNAP), which requires states to report lottery and gambling winnings and establish agreements with gaming entities to identify ineligible participants.
Department of Commerce Requests Public Comment on Direct Investment Surveys
The Department of Commerce is seeking public input on its proposed and ongoing information collections, including the Annual Survey of U.S. Direct Investment Abroad, as part of its effort to reduce the burden on the public and assess the impact of its data collection requirements.
US Department of Commerce Seeks Applicants for American Fisheries Advisory Committee
The US Department of Commerce is currently accepting applications for 7 membership positions on the 22-member American Fisheries Advisory Committee, with selected individuals serving a three-year term
U.S. Navy Gets Permission to Harm Marine Mammals for Norfolk Navy Project
The U.S. Navy has been granted permission to harm marine mammals as part of its repair and replacement project at Naval Station Norfolk in Norfolk, Virginia, in accordance with the Marine Mammal Protection Act.
Federal Agency Seeks Public Comment on Coral Reef Conservation Survey for South Florida
The U.S. government is requesting public input on a proposed survey to gather socioeconomics data on coral reef conservation in South Florida, with the goal of informing the 2026 survey
U.S. Department of Commerce Announces Final Results of Antidumping Duty Administrative Review for Ripe Olives From Spain
The U.S. Department of Commerce has concluded that certain Spanish producers/exporters sold olive products at below-market prices during the review period, August 1, 2022, through July 31, 2023.
U.S. Department of Commerce Announces Final Results and Partial Rescission of Countervailing Duty Administrative Review for CS Wind Malaysia Sdn Bhd
The U.S. Department of Commerce has determined that CS Wind Malaysia Sdn Bhd, a leading manufacturer of utility scale wind towers, received countervailable subsidies from January 1, 2022, through December 31, 2022, prompting a partial rescission of the administrative review.
U.S. Department of Commerce Publishes Final Results of Antidumping Duty Review on Stainless Steel Flanges from India
The U.S. Department of Commerce has released the final results of its 2022-2023 review of the antidumping duty order on stainless steel flanges imported from India, correcting a spelling error in a company name
U.S. Commerce Department Announces Final Results of Antidumping Review of Chinese Steel Nails
The U.S. Department of Commerce has determined that Shanghai Yueda Nails Co., Ltd. sold steel nails from China in the U.S. at prices below normal value during the review period, resulting in a final rescission of review for part of the subject merchandise.
U.S. Continues Antidumping Duty on Malleable Cast Iron Pipe Fittings from China
The U.S. Department of Commerce and the U.S. International Trade Commission have determined that revoking the antidumping duty order on malleable cast iron pipe fittings from China would likely lead to continued dumping and material injury to the U.S. industry, so the order will continue.
University of Washington et al submits application for duty-free entry of scientific instruments
The University of Washington, along with other institutions, has submitted an application to the US government for duty-free entry of scientific instruments, aiming to facilitate international collaborations and research in the field of science
U.S. Department of Commerce Preliminarily Determines Antidumping Duties on Chinese Wood Mouldings and Millwork Products
The U.S. Department of Commerce has found that Chinese exporters sold wood mouldings and millwork products at below-market prices during a recent review period, and is rescinding the review for 20 of the companies involved, leaving 18 companies subject to antidumping duties.
U.S. Commerce Department Announces Final Results of Antidumping Duty Review for Mexican Light-Walled Rectangular Pipe and Tube
The U.S. Department of Commerce has concluded that Mexican light-walled rectangular pipe and tube was sold in the U.S. at a price lower than its normal value during the review period, August 1, 2022, through July 31, 2023.