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Federal regulations

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    Recency
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    DHSRemove filter: DHSDOJRemove filter: DOJFAARemove filter: FAAFCCRemove filter: FCCFDARemove filter: FDAHUDRemove filter: HUDNIHRemove filter: NIHNOAARemove filter: NOAASBARemove filter: SBAUSDARemove filter: USDAClear all
    • 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.

    • United States et al. v. Live Nation Entertainment, Inc.; Proposed Final Judgment and Competitive Impact Statement
      July 6, 2026

      Proposed Final Judgment in US antitrust case against Live Nation Entertainment requires the company to divest certain assets and comply with operational restrictions affecting ticket sales and venue management; final judgment pending court approval.

    • Submission for OMB Review; Comment Request
    Page 1 of 80 (799 total)Next

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    July 6, 2026

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

  • 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; 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.

  • 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.

  • 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.

  • Atlantic Highly Migratory Species; Atlantic Bluefin Tuna Fisheries; Closure of the Angling Category Southern New England Area Trophy Fishery for 2026
    July 6, 2026

    NMFS closes the Atlantic bluefin tuna angling category trophy fishery in Southern New England for 2026 for fish measuring 73 inches or greater curved fork length.

  • 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.

  • 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.

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