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

Federal regulations

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    Recency
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    CMSRemove filter: CMSEPARemove filter: EPAFAARemove filter: FAAFCCRemove filter: FCCFDARemove filter: FDAIRSRemove filter: IRSNOAARemove filter: NOAASBARemove filter: SBAUSDARemove filter: USDAClear all
    • Determination That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness
      July 6, 2026

      FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.

    • Endo Operations Limited, et al.; Withdrawal of Approval of 34 New Drug Applications
      July 6, 2026

      FDA withdraws approval of 34 new drug applications across multiple applicants whose manufacturers requested withdrawal due to discontinued marketing.

    • Submission for OMB Review; Comment Request
    PreviousPage 2 of 63 (621 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.

  • 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.

  • 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.

  • Airworthiness Directives; Airbus Helicopters
    July 6, 2026

    FAA airworthiness directive requires Airbus Helicopters Model H160-B operators to modify affected windows in jettisoning systems and prohibits installation of non-conforming windows or doors on helicopters with Supplemental Type Certificate SR00223I…

  • Ensuring Passenger Safety by Preempting Duty and Rest Requirements
    July 6, 2026

    FAA proposes to clarify that federal flightcrew and flight attendant duty and rest regulations preempt all state and local meal and rest break requirements under the Airline Deregulation Act of 1978.

  • 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.

  • 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.

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