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

Federal regulations

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    Recency
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    CMSRemove filter: CMSEPARemove filter: EPAFAARemove filter: FAAFDARemove filter: FDAFTCRemove filter: FTCIRSRemove filter: IRSUSDARemove filter: USDAClear 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That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness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      FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.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.

    • Information Collection Request; General Program Administration
    PreviousPage 2 of 50 (500 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.

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    July 6, 2026

    Farm Service Agency seeks public comments on a revised information collection for General Program Administration to verify applicant eligibility, authorized loan use, and government security interests under the Paperwork Reduction Act.

  • Submission for OMB Review; Comment Request
    July 6, 2026

    OMB review process for federal regulations requires public comment submissions; the comment period deadline and specific regulatory details are not specified in the title alone.

  • Airworthiness Directives; Rolls-Royce Deutschland Ltd & Co KG Engines
    July 6, 2026

    The FAA proposes to supersede Airworthiness Directive 2009-04-13 for Rolls-Royce Deutschland BR700 series engines, requiring operators to revise engine maintenance programs to incorporate manufacturer-issued time limits for life-limited parts.

  • 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; Proposed Collection; Comment Request; Biologics License Applications, Procedures and Requirements
    July 6, 2026

    FDA seeks 60 days of public comment on information collection requirements for Biologics License Applications under the Paperwork Reduction Act; deadline for comments is 60 days from Federal Register publication.

  • Amendment of Using Agency and Controlling Agency for Restricted Areas R-5301, R-5302A, R-5302B, and R-5302C; NC
    July 6, 2026

    North Carolina amends the using and controlling agency designations for restricted airspace areas R-5301, R-5302A, R-5302B, and R-5302C without changing boundaries, altitudes, or operational parameters.

  • 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.

  • Organic Certification Cost Share Program (OCCSP)
    July 6, 2026

    The Organic Certification Cost Share Program (OCCSP) provides federal cost-sharing assistance for organic certification expenses to eligible producers and handlers through FSA county offices for fiscal years 2025 through 2031.

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