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© 2026 BizmoonPrivacyTermsCredits
  1. Home
  2. Regulations
  3. Federal
  4. Page 2

Federal regulations

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    • Compliance2
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    Recency
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    CMSRemove filter: CMSDOJRemove filter: DOJEPARemove filter: EPAFCCRemove filter: FCCFDARemove filter: FDANIHRemove filter: NIHClear 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That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness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      FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.

    • Privacy Act of 1974; Matching Program
    PreviousPage 2 of 47 (461 total)Next

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    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.

  • 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.

  • Proposed Collection; 60-day Comment Request; Generic Clearance for NIH Citizen Science and Crowdsourcing Projects (Office of the Director)
    July 6, 2026

    NIH requests 60-day public comment on proposed data collection for citizen science and crowdsourcing projects under Paperwork Reduction Act review; deadline is 60 days from publication.

  • Schedules of Controlled Substances: Temporary Placement of Mitragynine Pseudoindoxyl, MGM-15, and MGM-16 in Schedule I
    July 6, 2026

    The Drug Enforcement Administration announces temporary scheduling of mitragynine pseudoindoxyl, MGM-15, and MGM-16 as Schedule I controlled substances, restricting manufacturing, distribution, possession, and research activities.

  • Pesticide Product Registration; Receipt of Applications for New Active Ingredients (April 2026)
    July 6, 2026

    EPA accepts public comments on new pesticide product registration applications containing previously unregistered active ingredients, with details on 2025 submissions under Federal Insecticide, Fungicide, and Rodenticide Act procedures.

  • Pesticide Product Registration; Receipt of Applications for New Uses (April 2026)
    July 6, 2026

    EPA received pesticide product registration applications for new uses of currently registered active ingredients and solicits public comments on the April 2026 compilations.

  • 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.

  • Information Collection Being Reviewed by the Federal Communications Commission Under Delegated Authority
    July 6, 2026

    Federal Communications Commission invites public comment on information collection requirements under the Paperwork Reduction Act, with specific focus on reducing burdens for small businesses with fewer than 25 employees.

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