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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 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.
authority:
21 U.S.C. 321
,
351
,
352
,
353
,
355
,
356c
,
356e
,
360
,
360
i,
371
,
374
,
379k
;
42 U.S.C. 216
,
262
,
263
,
263
a,
264
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