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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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    DOERemove filter: DOEFCCRemove filter: FCCFDARemove filter: FDAFTCRemove filter: FTCNOAARemove filter: NOAASBARemove filter: SBAUSDARemove filter: USDAClear all
    • Expedited Investigational New Drug Pilot Program; Request for Information; Correction
      July 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.

    • Combined Notice of Filings #1
      July 6, 2026

      I need the description to create the summary. Please provide the description field for "Combined Notice of Filings #1."

    • 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That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness
    PreviousPage 2 of 55 (548 total)Next

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    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    FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.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.

  • 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; 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.

  • Implementing Voluntary Agreements Under the Defense Production Act
    July 6, 2026

    Department of Energy approves the Nuclear Fuel Cycle Consortium Voluntary Agreement under the Defense Production Act following public comment and interagency consultation.

  • Administrative Declaration of a Disaster for the State of New York
    July 6, 2026

    New York's Administrative Declaration of Disaster dated June 30, 2026, covers severe storms and flooding and may trigger state and federal disaster assistance programs for affected small businesses.

  • Records Governing Off-the-Record Communications; Public Notice
    July 6, 2026

    FCC public notice clarifies records requirements for off-the-record communications with agency staff, affecting broadcasters and telecommunications firms subject to FCC jurisdiction.

  • Powerhouse Systems, LLC; Notice of Intent To Prepare an Environmental Assessment
    July 6, 2026

    Powerhouse Systems, LLC must prepare an environmental assessment for a proposed project subject to federal review and public comment procedures.

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