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© 2026 BizmoonPrivacyTermsCredits
  1. Home
  2. Regulations
  3. Federal
  4. Page 2

Federal regulations

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  • Topic
    • Compliance2
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    Recency
    • Last 30 days
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    CMSRemove filter: CMSDOLRemove filter: DOLFAARemove filter: FAAFCCRemove filter: FCCFDARemove filter: FDAFTCRemove filter: FTCIRSRemove filter: IRSNIHRemove filter: NIHNOAARemove filter: NOAAClear all
    • 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That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness
      July 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      FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.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 Applications
      July 6, 2026

      FDA withdraws approval of 34 new drug applications across multiple applicants whose manufacturers requested withdrawal due to discontinued marketing.

    • Privacy Act of 1974; Matching Program
    PreviousPage 2 of 55 (542 total)Next

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    Healthcare draws more federal rulemaking than any other sector

    After healthcare come the capital-heavy sectors: trade, transportation, energy, and finance. If you operate in one of them, the volume of change is relentless.

    Federal rulemaking

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    July 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.

  • Ensuring Passenger Safety by Preempting Duty and Rest Requirements
    July 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.

  • Information Collection Being Reviewed by the Federal Communications Commission Under Delegated Authority
    July 6, 2026

    Federal Communications Commission invites public comment on information collection requirements under the Paperwork Reduction Act, with specific focus on reducing burdens for small businesses with fewer than 25 employees.

  • Proposed Collection; 60-day Comment Request; Generic Clearance for NIH Citizen Science and Crowdsourcing Projects (Office of the Director)
    July 6, 2026

    NIH requests 60-day public comment on proposed data collection for citizen science and crowdsourcing projects under Paperwork Reduction Act review; deadline is 60 days from publication.

  • Airworthiness Directives; Airbus Helicopters
    July 6, 2026

    FAA airworthiness directive requires inspection and repair of missing retaining rings on jettisonable window hinge pins for Airbus Helicopters Model H160-B helicopters.

  • Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Administrative Practices and Procedures; Formal Hearings
    July 6, 2026

    FDA submitted a proposed information collection to OMB for Paperwork Reduction Act review regarding formal hearing administrative procedures and practices.

  • Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Premarket Approval of Medical Devices
    July 6, 2026

    The FDA seeks OMB clearance for information collection procedures related to premarket approval of medical devices under the Paperwork Reduction Act.

  • Petition for Reconsideration of Action in Rulemaking Proceeding
    July 6, 2026

    DIRECTV, LLC filed a Petition for Reconsideration with the Commission through representative Brenna Sparks regarding a rulemaking proceeding action.

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