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

Federal regulations

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  • Recency
    • Last 30 days
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    CMSRemove filter: CMSDOLRemove filter: DOLFCCRemove filter: FCCFDARemove filter: FDAFTCRemove filter: FTCHHSRemove filter: HHSNIHRemove filter: NIHClear all
    • 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.

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

      CDC seeks public comment on a data collection for mChoice, a research study testing tailored provider training and adherence support to improve PrEP uptake among young men who have sex with men in high-priority settings.

    • Information Collection Being Reviewed by the Federal Communications Commission Under Delegated Authority
    PreviousPage 2 of 43 (423 total)Next

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    Healthcare draws more federal rulemaking than any other sector

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    July 6, 2026

    Federal Communications Commission invites public comment on information collection requirements under the Paperwork Reduction Act, with specific focus on reducing burdens for small businesses with fewer than 25 employees.

  • 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.

  • 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.

  • 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.

  • 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.

  • 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.

  • Patient Safety Organizations: Voluntary Relinquishment for the Cassatt Patient Safety Organization
    July 6, 2026

    AHRQ delisted Cassatt Patient Safety Organization (PSO number P0136) following its voluntary relinquishment of patient safety organization status under the Patient Safety and Quality Improvement Act.

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