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US law
Federal (United States)
Regulations
Title 21 CFR — Food and Drugs
Chapter I
Part 312
Subpart C
Federal (United States) · Regulations
Subpart C
5 sections
5 sections
21 C.F.R. § 312.40
General requirements for use of an investigational new drug in a clinical investigation.
21 C.F.R. § 312.41
Comment and advice on an IND.
21 C.F.R. § 312.42
Clinical holds and requests for modification.
21 C.F.R. § 312.45
Inactive status.
21 C.F.R. § 312.48
Dispute resolution.
Subpart C | Federal (United States) Regulations | Justis AI