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7/30/2026

National Institutes of Health Announces Amended Meeting Notice

The Office of the Director at the National Institutes of Health has issued an amended notice regarding a meeting, which may involve discussions and decisions by a committee or other governing body, and may be subject to certain rules or regulations, and may be open to the public or restricted to certain individuals or groups.

7/30/2026

FDA Announces Prescription Drug User Fee Rates for Fiscal Year 2027

The Food and Drug Administration is setting the rates for prescription drug user fees for the upcoming fiscal year, following the Prescription Drug User Fee Amendments of 2022, which gave the agency the authority to collect fees for certain applications and approved products.

7/30/2026

Animal Generic Drug User Fee Program Rates and Payment Procedures for Fiscal Year 2027

The Food and Drug Administration is announcing the fee rates and payment procedures for fiscal year 2027 generic new animal drug program user fees, as mandated by the Animal Generic Drug User Fee Amendments of 2023. The FDA is establishing the fee rates for FY 2027, following the amendments to the Federal Food, Drug, and Cosmetic Act.

7/30/2026

Outsourcing Facility Fee Rates for Fiscal Year 2027

The Food and Drug Administration (FDA) has announced the fiscal year 2027 rates for establishment and reinspection fees for outsourcing facilities that compound human drugs and register under the Federal Food, Drug, and Cosmetic Act. The rates include a small business establishment fee of $7,142, a non-small business establishment fee of $22,074, and a reinspection fee of $21,427.

7/30/2026

FDA Announces Generic Drug User Fee Rates for Fiscal Year 2027

The US Food and Drug Administration (FDA) has published the fiscal year 2027 rates for fees related to the review of generic drugs, as mandated by the Generic Drug User Fee Amendments of 2022 (GDUFA III). These fees will be used to support the agency's efforts to review and approve generic drug applications.

7/30/2026

FDA Announces 2027 VQIP User Fee Rate

The FDA is setting an annual fee for importers participating in the Voluntary Qualified Importer Program, which is part of the Food Safety Modernization Act, starting August 1, 2026, and ending September 30, 2027.

7/30/2026

FDA Announces Biosimilar User Fee Rates for Fiscal Year 2027

The US Food and Drug Administration (FDA) has announced the user fee rates for biosimilar biological products for fiscal year 2027, as mandated by the Biosimilar User Fee Amendments of 2022 (BsUFA III). The rates will cover various activities, including development, review, and approval of biosimilar products.

7/30/2026

Medicare Program; Updates to the Master List of Items Potentially Subject to Face-to-Face Encounter and Written Order Prior to Delivery and/or Prior Authorization Requirements; Updates to the Required Face-to-Face Encounter and Written Order Prior to Delivery List; and Updates to the Required Prior Authorization List

The Centers for Medicare & Medicaid Services (CMS) has released updates to the Master List of items potentially subject to face-to-face encounter and written order prior to delivery and/or prior authorization requirements. These updates also affect the Required Face-to-Face Encounter and Written Order Prior to Delivery List and the Required Prior Authorization List.

7/30/2026

Toyota Motor North America Receives NHTSA Petition for Decision on Noncompliance

Toyota Motor North America, Inc. has submitted a petition to the National Highway Traffic Safety Administration (NHTSA) regarding noncompliance with Federal Motor Vehicle Safety Standard (FMVSS) No. 209, citing Joyson Safety Systems Seat Belt Assemblies. The petition, filed on December 6, 2024, seeks a determination that the noncompliance is inconsequential to motor vehicle safety.

7/30/2026

DOT Proposes Update to Physiological Training System of Records Notice

The Department of Transportation (DOT) is proposing to update and reissue a system of records notice related to physiological training, changing its title from 'Department of Transportation, Federal Aviation Administration, DOT/FAA 828 Physiological Training System' to 'DOT/FAA 828 Physiological Training Records'.

7/30/2026

FAA Issues Revised Airworthiness Directive for Bell Textron Canada Limited Helicopters

The Federal Aviation Administration (FAA) has superseded Airworthiness Directive (AD) 2024-02-55, which applies to certain Bell Textron Canada Limited (BTCL) Model 505 helicopters, requiring inspections and corrective actions to address an unsafe condition, and introduces a new design for the vertical stabilizer top end cap assembly.

7/30/2026

FAA Adopts New Airworthiness Directive for Bombardier Aircraft

The Federal Aviation Administration (FAA) has issued a new airworthiness directive (AD) for Bombardier, Inc.'s Model BD-700-1A10 and BD-700-1A11 airplanes, requiring inspections and replacements of affected brake control units due to a main landing gear tire burst incident.

7/30/2026

FAA Adopts New Airworthiness Directive for Airbus A330-841 and A330-941 Airplanes

The Federal Aviation Administration (FAA) has issued a new airworthiness directive (AD) for Airbus SAS Model A330-841 and Model A330-941 airplanes, requiring repetitive inspections and corrective actions due to reports of crack findings on the sloping rib, in an effort to address an unsafe condition on these aircraft.

7/30/2026

FMCSA Withdraws Exemption Renewal Notice for Charles Machine Works, Inc. Due to Final Rule Providing Relief

The Federal Motor Carrier Safety Administration (FMCSA) has withdrawn its January 16, 2026, notice requesting public comment on an application from Charles Machine Works, Inc. (CMW) to renew a five-year exemption from the prohibition on gravity-fed or siphon-fed fuel systems on commercial motor vehicles (CMVs), as the February 19, 2026, final rule addressing 'Parts and Accessories Necessary for Safe Operation; Auxiliary Fuel Tanks' already provided the necessary relief, rendering the exemption unnecessary for CMW and potentially other entities.

7/30/2026

USDA NRCS Announces Record of Decision for Clarke County Water Supply Project in Iowa

The US Department of Agriculture's Natural Resources Conservation Service (NRCS) has selected a preferred alternative for the Clarke County Water Supply Project, which includes constructing a reservoir with a dam, installing a water pipeline, and relocating a local road, as outlined in the Final Plan-Environmental Impact Statement (EIS) and Record of Decision (ROD) for the project in Clarke County, Iowa.