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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: CMSFCCRemove filter: FCCFDARemove filter: FDAFTCRemove filter: FTCHUDRemove filter: HUDNIHRemove filter: NIHTreasuryRemove filter: TreasuryUSDARemove filter: USDAClear all
    • 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.

    • Extension of a Currently Approved Information Collection: Certificate of Identity
      July 6, 2026

      Department of the Treasury Bureau of Fiscal Service seeks public comment on the Certificate of Identity information collection under the Paperwork Reduction Act of 1995.

    • 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That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness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 46 (451 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

    FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.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

  • Prohibiting Importation and Marketing of Previously Authorized Covered Communications Equipment Added to the Covered List in 2024 or Earlier
    July 6, 2026

    The FCC prohibits importation and marketing of communications equipment designated as covered products in 2024 or earlier due to national security risks.

  • Extension of a Currently Approved Information Collection: Special Form of Request for Payment of US Savings and Retirement Securities Where Use of a Detached Request Is Authorized
    July 6, 2026

    The Treasury Department's Bureau of the Fiscal Service requests public comment on its Special Form for requesting payment of US savings and retirement securities, extending the current Paperwork Reduction Act collection through the specified approva…

  • Privacy Act of 1974; System of Records
    July 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.

  • 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.

  • Section 8 Housing Assistance Payments Program-Fiscal Year (FY) 2026 Inflation Factors for Public Housing Agency (PHA) Renewal Funding
    July 6, 2026

    HUD establishes FY 2026 Renewal Funding Inflation Factors averaging 2.337 percent to adjust Housing Choice Voucher program allocations for public housing agencies based on local Fair Market Rent changes.

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