21 C.F.R. § 812.42

FDA and IRB approval.

Last amended: 2016Year: 2026Length: 40 wordsOfficial source

Cite as 21 C.F.R. § 812.42 (2026)

A sponsor shall not begin an investigation or part of an investigation until an IRB and FDA have both approved the application or supplemental application relating to the investigation or part of an investigation. [46 FR 8957, Jan. 27, 1981]
21 C.F.R. § 812.42: FDA and IRB approval. | Justis AI