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  1. Home
  2. Regulations
  3. Federal
  4. Page 2

Federal regulations

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    Recency
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    DOJRemove filter: DOJDOTRemove filter: DOTEPARemove filter: EPAFAARemove filter: FAAFDARemove filter: FDAIRSRemove filter: IRSClear all
    • 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.

    • 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That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness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      FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.

    PreviousPage 2 of 59 (585 total)Next

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    Healthcare draws more federal rulemaking than any other sector

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    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.

  • Ensuring Passenger Safety by Preempting Duty and Rest Requirements
    July 6, 2026

    FAA proposes to clarify that federal flightcrew and flight attendant duty and rest regulations preempt all state and local meal and rest break requirements under the Airline Deregulation Act of 1978.

  • 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.

  • Request Notice: Use of Foreign-Built Small Passenger Vessel in United States Coastwise Trade, M/V DEUCE
    July 6, 2026

    MARAD is soliciting public comments on a request to operate the foreign-built vessel M/V DEUCE in U.S. coastwise trade carrying no more than twelve passengers for hire, to assess potential impacts on U.S. vessel builders and coastwise trade operator…

  • Request Notice: Use of Foreign-Built Small Passenger Vessel in United States Coastwise Trade, M/V MEAT WAGON 2
    July 6, 2026

    The Maritime Administration invites public comments on a determination request for the foreign-built M/V MEAT WAGON 2 to operate in U.S. coastwise trade carrying up to twelve passengers for hire.

  • Request Notice: Use of Foreign-Built Small Passenger Vessel in United States Coastwise Trade, S/V NAUTI DOG
    July 6, 2026

    MARAD is soliciting public comment on a request to use foreign-built passenger vessel S/V NAUTI DOG in U.S. coastwise trade carrying no more than twelve passengers for hire.

  • 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.

  • Rivian Automotive, LLC, Grant of Petition for Decision of Inconsequential Noncompliance
    July 6, 2026

    NHTSA grants Rivian's petition that MY 2022 electric delivery van noncompliance with Federal Motor Vehicle Safety Standard No. 208 is inconsequential to motor vehicle safety.

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