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  1. Home
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Federal regulations

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    Recency
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    DOJRemove filter: DOJEPARemove filter: EPAFCCRemove filter: FCCFDARemove filter: FDANIHRemove 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.

    • 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.

    • United States et al. v. Live Nation Entertainment, Inc.; Proposed Final Judgment and Competitive Impact Statement
    Page 1 of 55 (550 total)Next

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    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.

  • 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
    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.

  • 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.

  • Receipt of Pesticide Petitions Filed for Residues of Pesticide Chemicals in or on Various Commodities-April 2026
    July 6, 2026

    EPA announces receipt of pesticide residue petitions for various commodities and opens public comment period; petitions filed in 2025 and 2026 are under evaluation for regulatory establishment or modification.

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