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  1. Home
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Federal regulations

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    CMSRemove filter: CMSDOTRemove filter: DOTFDARemove filter: FDAFTCRemove filter: FTCHUDRemove filter: HUDIRSRemove filter: IRSClear 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.

    • Request Notice: Use of Foreign-Built Small Passenger Vessel in United States Coastwise Trade, S/V PURPLE PELICAN
      June 18, 2026

      MARAD is soliciting comments on a request to operate the foreign-built vessel S/V Purple Pelican in U.S. coastwise trade carrying up to twelve passengers for hire to assess potential adverse effects on U.S. vessel builders and domestic maritime oper…

    • 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
    Page 1 of 40 (400 total)Next

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    Healthcare draws more federal rulemaking than any other sector

    After healthcare come the capital-heavy sectors: trade, transportation, energy, and finance. If you operate in one of them, the volume of change is relentless.

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    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.

  • 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.

  • Denial of Motor Vehicle Defect Petition, DP21-003
    June 18, 2026

    NHTSA denied petition DP21-003 requesting investigation of alleged runaway throttle and speed control defects in Kia and Hyundai vehicles, finding insufficient evidence that accelerator systems violate Federal Motor Vehicle Safety Standards.

  • Request for Information Regarding Products and Categories of Products Used in Housing Programs Pursuant to the Build America, Buy America Act
    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.

  • Agency Information Collection Activities; Notice and Request for Comment; Assessment of Contextual Driver Monitoring Systems (DMS); Correction
    June 18, 2026

    NHTSA corrects the docket number in its June 10, 2026 Federal Register notice requesting comment on contextual driver monitoring systems assessment procedures.

  • Pipeline Safety: Information Collection Activities
    June 18, 2026

    PHMSA seeks comments on revised incident, accident, and annual report forms for gas and hazardous liquid pipeline facilities plus the National Pipeline Mapping System under the Paperwork Reduction Act.

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