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Federal regulations

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    CMSRemove filter: CMSDHSRemove filter: DHSDOCRemove filter: DOCFDARemove filter: FDAHUDRemove filter: HUDNIHRemove filter: NIHClear all
    • Clover Hill Dairy Expands Recall to Include All Clover Hill Dairy Brand Cheese Due to Possible Health Risk
      June 18, 2026

      Clover Hill Dairy of Mechanicsville, Maryland recalls all Clover Hill Dairy brand cheese due to potential Listeria monocytogenes contamination; recall effective June 18, 2026.

    • 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.

    • Request for Information Regarding Products and Categories of Products Used in Housing Programs Pursuant to the Build America, Buy America Act
    Page 1 of 59 (583 total)Next

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  • June 18, 2026

    HUD seeks public input on the availability of domestically manufactured products for federally funded housing and infrastructure projects under the Build America, Buy America Act.

  • 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.

  • Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Current Good Manufacturing Practice Regulations for Type A Medicated Articles and Medicated Feeds
    June 18, 2026

    FDA requests OMB clearance for information collection activities related to Current Good Manufacturing Practice regulations for Type A medicated articles and medicated feeds under the Paperwork Reduction Act of 1995.

  • Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements
    June 18, 2026

    FDA submission to OMB for Paperwork Reduction Act review of information collection requirements for dietary supplement manufacturing, packaging, labeling, and holding operations.

  • 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.

  • Raw Honey from India: Final Results of Antidumping Duty Administrative Review; 2023-2024
    June 18, 2026

    U.S. Commerce Department finds raw honey imports from India sold below normal value during June 1, 2023–May 31, 2024, triggering antidumping duty considerations for affected U.S. honey producers and importers.

  • Agency Information Collection Activities: Submission for OMB Review; Comment Request
    June 18, 2026

    CMS is requesting public comment on proposed information collection activities under the Paperwork Reduction Act; interested parties may submit feedback on burden estimates and collection methods.

  • 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.

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