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Regulations last checked for updates: May 14, 2025

Title 21 - Food and Drugs last revised: May 12, 2025
All TitlesTitle 21Chapter IPart 803Subpart C - Subpart C—User Facility Reporting Requirements
  • § 803.30 - If I am a user facility, what reporting requirements apply to me?
  • § 803.32 - If I am a user facility, what information must I submit in my individual adverse event reports?
  • § 803.33 - If I am a user facility, what must I include when I submit an annual report?
authority: 21 U.S.C. 352,360,360i,360j,371,374
source: 79 FR 8846, Feb. 14, 2014, unless otherwise noted.
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