42 C.F.R. § 11.20

Who must submit clinical trial registration information?

Last amended: 2017Year: 2026Length: 22 wordsOfficial source

Cite as 42 C.F.R. § 11.20 (2026)

The responsible party for an applicable clinical trial specified in § 11.22 must submit clinical trial registration information for that clinical trial.
Cross-references to the CFR
11.22
42 C.F.R. § 11.20: Who must submit clinical trial registration information? | Justis AI