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Federal regulations

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    • 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.

    • Information Collection Requests; Emergency Conservation Program (ECP) and Biomass Crop Assistance Program (BCAP)
      June 18, 2026

      Farm Service Agency requests public comments on revised information collection requirements for Emergency Conservation Program and Biomass Crop Assistance Program eligibility, cost-share agreements, and payment certification.

    • Finished Carbon Steel Flanges From India: Final Results of Antidumping Duty Administrative Review; 2023-2024
      June 18, 2026

      The U.S. Department of Commerce finds finished carbon steel flanges from India were dumped in the United States during August 1, 2023 through July 31, 2024, triggering antidumping duty assessments.

    • 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.

    • 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.

    • 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.

    • 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.

    • 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.

    • 30-Day Notice of Proposed Information Collection: Housing Opportunity Through Modernization Act of 2016 (HOTMA): Public Housing Waiting List Data Collection Tool
      June 18, 2026

      HUD seeks OMB approval for a public housing waiting list data collection tool under the Housing Opportunity Through Modernization Act; public comment period ends 30 days from publication.

    • 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.

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