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  1. Home
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Federal regulations

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    Recency
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    CMSRemove filter: CMSDHSRemove filter: DHSDOLRemove filter: DOLEPARemove filter: EPAFCCRemove filter: FCCFDARemove filter: FDAFTCRemove filter: FTCHUDRemove filter: HUDNIHRemove filter: NIHSBARemove filter: SBAUSDARemove filter: USDAClear all
    • Submission for OMB Review; Comment Request
      July 6, 2026

      I need the description to create an accurate summary. Please provide the description field for this OMB submission document.

    • Privacy Act of 1974; Matching Program
      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.

    • 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That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness
    Page 1 of 71 (710 total)Next

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    Healthcare draws more federal rulemaking than any other sector

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    FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.

  • Safety Zone; Lake Michigan, Chicago, IL
    July 6, 2026

    Coast Guard establishes temporary safety zone in Monroe Harbor and Lake Michigan near Chicago to prohibit unauthorized vessel and personnel access during fireworks and drone show operations.

  • Information Collection Request; General Program Administration
    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.

  • 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.

  • 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.

  • 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.

  • 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.

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