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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: CMSFCCRemove filter: FCCFDARemove filter: FDAFTCRemove filter: FTCHUDRemove filter: HUDIRSRemove 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That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness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      FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.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 45 (444 total)Next

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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.

  • Notice of Regulatory Waiver Requests Granted for the Fourth Quarter of Calendar Year 2025
    July 6, 2026

    HUD publishes regulatory waivers granted during the fourth quarter of 2025 (October 1 through December 31) as required by Section 106 of the HUD Reform Act.

  • Notice of Regulatory Waiver Requests Granted for the Third Quarter of Calendar Year 2025
    July 6, 2026

    HUD published regulatory waivers granted during the third quarter of 2025 (July 1–September 30) in compliance with the HUD Reform Act's quarterly Federal Register notice requirement.

  • 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.

  • 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.

  • Information Collection Being Reviewed by the Federal Communications Commission
    July 6, 2026

    The FCC invites public comment on information collection requirements under the Paperwork Reduction Act, with specific focus on reducing compliance burden for small businesses with fewer than 25 employees.

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