Federal regulations
- Privacy Act of 1974; Matching ProgramJuly 6, 2026
Centers for Medicare & Medicaid Services launches a matching program with the Department of Veterans Affairs to verify eligibility for insurance affordability programs under the Affordable Care Act.
- Privacy Act of 1974; System of RecordsJuly 6, 2026
HUD rescinded its One Stop Customer Service Privacy Act system of records as of October 30, 2024, consolidating functions into its Customer Relationship Management system.
- Determination That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or EffectivenessJuly 6, 2026
FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.
- Endo Operations Limited, et al.; Withdrawal of Approval of 34 New Drug ApplicationsJuly 6, 2026
FDA withdraws approval of 34 new drug applications across multiple applicants whose manufacturers requested withdrawal due to discontinued marketing.
- Agency Forms Undergoing Paperwork Reduction Act ReviewJuly 6, 2026
Multiple federal agency forms are undergoing Paperwork Reduction Act review to assess and potentially reduce reporting burdens on small businesses and other respondents.
- Ensuring Passenger Safety by Preempting Duty and Rest RequirementsJuly 6, 2026
FAA proposes to clarify that federal flightcrew and flight attendant duty and rest regulations preempt all state and local meal and rest break requirements under the Airline Deregulation Act of 1978.
- Expedited Investigational New Drug Pilot Program; Request for Information; CorrectionJuly 6, 2026
FDA corrects contact information for the Expedited Investigational New Drug Pilot Program docket, which solicits public input on shortening timelines from drug identification to first-in-human clinical trials.
- Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Premarket Approval of Medical DevicesJuly 6, 2026
The FDA seeks OMB clearance for information collection procedures related to premarket approval of medical devices under the Paperwork Reduction Act.
- Temporary Placement of 7-Hydroxymitragynine Above a Specified Threshold in Schedule I; Request for InformationJuly 6, 2026
The Office of the Assistant Secretary for Health seeks public comments on a proposed threshold for scheduling 7-hydroxymitragynine under the Controlled Substances Act.
- Airworthiness Directives; Airbus HelicoptersJuly 6, 2026
FAA airworthiness directive requires Airbus Helicopters Model H160-B operators to modify affected windows in jettisoning systems and prohibits installation of non-conforming windows or doors on helicopters with Supplemental Type Certificate SR00223I…
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Healthcare draws more federal rulemaking than any other sector
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Federal rulemaking
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- Energy and utilities
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