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Regulations last checked for updates: Feb 11, 2026
Title 21 - Food and Drugs last revised: Dec 18, 2026
All Titles
Title 21
Chapter I
Part 230
Subpart C - Subpart C—Postmarketing Quality and Safety Reporting
§ 230.205 - Field alert reports.
§ 230.210 - General reporting requirements for designated medical gas adverse events.
§ 230.220 - Human designated medical gas ICSR requirements.
§ 230.230 - Animal designated medical gas adverse event reporting requirements.
authority:
21 U.S.C. 321
,
331
,
351
,
352
,
353
,
355
,
355
a,
355
f,
356
,
356
a,
356
b,
356
c,
356
e,
360b
,
360cc
,
360ddd
,
360ddd
-1,
371
,
374
,
379e
,
379k
,
381
source:
89 FR 51777, June 18, 2024, unless otherwise noted.
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