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VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or Effectiveness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      FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.

    • Temporary Placement of 7-Hydroxymitragynine Above a Specified Threshold in Schedule I; Request for Information
      July 6, 2026

      The Office of the Assistant Secretary for Health seeks public comments on a proposed threshold for scheduling 7-hydroxymitragynine under the Controlled Substances Act.

    • Submission for OMB Review; Comment Request
    PreviousPage 2 of 51 (509 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 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; Submission for Office of Management and Budget Review; Comment Request; Administrative Practices and Procedures; Formal Hearings
    July 6, 2026

    FDA submitted a proposed information collection to OMB for Paperwork Reduction Act review regarding formal hearing administrative procedures and practices.

  • Agency Information Collection Activities: Submission for OMB Review; Comment Request
    July 6, 2026

    Federal agencies submit information collection requests to OMB for review and public comment to assess burden on businesses and the public.

  • Privacy Act of 1974; System of Records
    July 6, 2026

    HUD rescinded its One Stop Customer Service Privacy Act system of records as of October 30, 2024, consolidating functions into its Customer Relationship Management system.

  • 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.

  • Proposed Data Collection Submitted for Public Comment and Recommendations
    July 6, 2026

    CDC seeks public comment through [date] on the Expanding PrEP in Communities of Color (EPICC) data collection effort, which supports shared decision-making training and evaluation for preexposure prophylaxis providers serving diverse populations.

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