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Regulations last checked for updates: Jul 12, 2025
Title 21 - Food and Drugs last revised: Jun 26, 2025
All Titles
Title 21
Chapter I
Part 600
Subpart D - Subpart D—Reporting of Adverse Experiences
§ 600.80 - Postmarketing reporting of adverse experiences.
§ 600.81 - Distribution reports.
§ 600.82 - Notification of a permanent discontinuance or an interruption in manufacturing.
§ 600.90 - Waivers.
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