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US law
Federal (United States)
Regulations
Title 21 CFR — Food and Drugs
Chapter I
Part 230
Subpart C
Federal (United States) · Regulations
Subpart C
4 sections
4 sections
21 C.F.R. § 230.205
Field alert reports.
21 C.F.R. § 230.210
General reporting requirements for designated medical gas adverse events.
21 C.F.R. § 230.220
Human designated medical gas ICSR requirements.
21 C.F.R. § 230.230
Animal designated medical gas adverse event reporting requirements.
Subpart C | Federal (United States) Regulations | Justis AI