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© 2026 BizmoonPrivacyTermsCredits
  1. Home
  2. Regulations
  3. Federal
  4. Page 3

Federal regulations

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    Recency
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    CMSRemove filter: CMSEPARemove filter: EPAFCCRemove filter: FCCFDARemove filter: FDAFTCRemove filter: FTCHHSRemove filter: HHSNIHRemove filter: NIHUSDARemove filter: USDAClear all
    • Expedited Investigational New Drug Pilot Program; Request for Information; Correction
      July 6, 2026

      FDA corrects contact information for the Expedited Investigational New Drug Pilot Program docket, which solicits public input on shortening timelines from drug identification to first-in-human clinical trials.

    • Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Premarket Approval of Medical Devices
      July 6, 2026

      The FDA seeks OMB clearance for information collection procedures related to premarket approval of medical devices under the Paperwork Reduction Act.

    • Submission for OMB Review; Comment Request
    PreviousPage 3 of 54 (533 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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    July 6, 2026

    I need the description to create an accurate summary. Please provide the description field for this OMB submission document.

  • Information Collection Request; General Program Administration
    July 6, 2026

    Farm Service Agency seeks public comments on a revised information collection for General Program Administration to verify applicant eligibility, authorized loan use, and government security interests under the Paperwork Reduction Act.

  • Privacy Act of 1974; Matching Program
    July 6, 2026

    Centers for Medicare & Medicaid Services launches a matching program with the Department of Veterans Affairs to verify eligibility for insurance affordability programs under the Affordable Care Act.

  • Agency Forms Undergoing Paperwork Reduction Act Review
    July 6, 2026

    Multiple federal agency forms are undergoing Paperwork Reduction Act review to assess and potentially reduce reporting burdens on small businesses and other respondents.

  • Prohibiting Importation and Marketing of Previously Authorized Covered Communications Equipment Added to the Covered List in 2024 or Earlier
    July 6, 2026

    The FCC prohibits importation and marketing of communications equipment designated as covered products in 2024 or earlier due to national security risks.

  • Agency Information Collection Activities; Proposed Collection; Comment Request; Biologics License Applications, Procedures and Requirements
    July 6, 2026

    FDA seeks 60 days of public comment on information collection requirements for Biologics License Applications under the Paperwork Reduction Act; deadline for comments is 60 days from Federal Register publication.

  • National Emission Standards for Hazardous Air Pollutants: Plywood and Composite Wood Products
    July 6, 2026

    EPA finalizes hazardous air pollutant emission standards for plywood and composite wood products facilities, setting maximum achievable control technology limits for formaldehyde, acetaldehyde, and other HAP compounds at major source facilities.

  • Petition for Reconsideration of Action in Rulemaking Proceeding
    July 6, 2026

    DIRECTV, LLC filed a Petition for Reconsideration with the Commission through representative Brenna Sparks regarding a rulemaking proceeding action.

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