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Federal regulations

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    Recency
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    DOCRemove filter: DOCFCCRemove filter: FCCFTCRemove filter: FTCHHSRemove filter: HHSNIHRemove filter: NIHClear all
    • Certain Chassis and Subassemblies Thereof From Mexico and Thailand: Countervailing Duty Orders
      June 18, 2026

      U.S. Department of Commerce issues countervailing duty orders on certain chassis and subassemblies from Mexico and Thailand following affirmative trade injury determinations.

    • Agency Forms Undergoing Paperwork Reduction Act Review
      June 18, 2026

      Federal agency forms are undergoing Paperwork Reduction Act review to assess burden on small businesses and other respondents.

    • Agency Forms Undergoing Paperwork Reduction Act Review
      June 18, 2026

      Federal agencies are reviewing multiple forms under the Paperwork Reduction Act to reduce burden on small businesses and other respondents.

    • Proposed Data Collection Submitted for Public Comment and Recommendations
      June 18, 2026

      CDC seeks public comment on the Public Health Emergency Management Tool data collection under the Paperwork Reduction Act of 1995 to assess emergency management capacity in partner countries.

    • Agency Forms Undergoing Paperwork Reduction Act Review
      June 18, 2026

      Federal agencies are reviewing multiple forms for paperwork reduction compliance under the Paperwork Reduction Act; public comment period open for burden reduction assessments.

    • Authorization of Emergency Use for Two Animal Drugs for the Prevention and Treatment of New World Screwworm; Availability
      June 18, 2026

      FDA issues Emergency Use Authorizations for two animal drugs to prevent and treat New World screwworm infestations in livestock, poultry, and exotic animals following HHS's August 18, 2025 public health emergency declaration.

    • SpecGx LLC; Withdrawal of Approval of Abbreviated New Drug Application for Methylphenidate Hydrochloride Extended-Release Tablets, 27 Milligrams, 36 Milligrams, and 54 Milligrams
      June 18, 2026

      FDA withdraws approval of SpecGx LLC's abbreviated new drug application for Methylphenidate Hydrochloride Extended-Release tablets in 27mg, 36mg, and 54mg strengths per the applicant's request.

    • Advisory Committee; Science Board to the Food and Drug Administration; Renewal
      June 18, 2026

      The FDA renews its Science Board advisory committee for an additional two years, with the new charter expiring June 26, 2028.

    • Foreign-Trade Zone 38; Application for Subzone; ElringKlinger South Carolina, LLC; Easley, South Carolina
      June 18, 2026

      Foreign-Trade Zone 38 subzone application for ElringKlinger South Carolina, LLC in Easley allows duty-free importation of automotive components for manufacturing and re-export.

    • Center for Scientific Review; Notice of Closed Meetings
      June 18, 2026

      Center for Scientific Review will hold closed meetings to review and discuss NIH grant applications and related administrative matters on specified dates.

    Page 1 of 45 (448 total)Next

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