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

Federal regulations

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    Recency
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    FDARemove filter: FDAHHSRemove filter: HHSClear all
    • Center for Scientific Review; Amended Notice of Meeting
      June 15, 2026

      Center for Scientific Review announces amended open meeting schedule to discuss peer review processes and grant evaluation procedures for National Institutes of Health funding cycles.

    • National Vaccine Injury Compensation Program; List of Petitions Received
      June 15, 2026

      HRSA publishes notice of petitions received under the National Vaccine Injury Compensation Program, which are adjudicated by the U.S. Court of Federal Claims per PHS Act requirements.

    • National Institute of Diabetes and Digestive and Kidney Diseases; Amended Notice of Meeting
      June 15, 2026

      National Institute of Diabetes and Digestive and Kidney Diseases announces an amended meeting notice for its advisory council to discuss research priorities and funding initiatives affecting small biotech and life-sciences firms.

    • Center for Scientific Review; Amended Notice of Meeting
      June 15, 2026

      Center for Scientific Review amends meeting notice regarding review panels and grant evaluation procedures for National Institutes of Health funding decisions.

    • Amendment and Revocation of Organizational Information Regulations
      June 15, 2026

      FDA amends regulations to direct the public to its website for organizational and contact information while revoking outdated regulations related to agency structure and contacts.

    • Request for Information; Comprehensive Review of the Essential Health Benefits Framework and Typical Employer Plan Standard
      June 15, 2026

      CMS seeks public comment on the Essential Health Benefits framework, State benchmark plans, and benefit scope methodologies to inform potential future regulatory revisions under the Affordable Care Act.

    • Forms FDA 3542a and FDA 3542: Questions and Answers; Draft Guidance for Industry; Availability
      June 15, 2026

      FDA draft guidance clarifies Forms FDA 3542a and 3542 submission requirements to assist industry applicants in preparing regulatory filings.

    • Government Owned Inventions Available for License: 4-Amino-2-(Piperidin-3-yl)Isoindoline-1,3-Diones as Anti-Inflammatory Agents for Systemic Degenerative and Neurodegenerative Disorders
      June 15, 2026

      National Institute on Aging offers licensing opportunities for 4-amino-2-(piperidin-3-yl)isoindoline-1,3-diones, pre-clinical anti-inflammatory compounds targeting systemic and neurodegenerative disorders, to qualified research and commercialization…

    • NARA ORGANICS RECALLS ALL LOTS OF NARA INFANT FORMULA BECAUSE OF POSSIBLE HEALTH RISK
      June 13, 2026

      Nara Organics recalls all lots of powdered infant formula nationwide due to potential Clostridium botulinum contamination posing risk of infant botulism.

    • Agency Forms Undergoing Paperwork Reduction Act Review
      June 12, 2026

      Federal agencies are reviewing multiple forms under the Paperwork Reduction Act to assess information collection burdens on small businesses and the public.

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