Federal (United States) · Regulations
Subpart C — Responsibilities of Sponsors
6 sections
6 sections
- 21 C.F.R. § 812.40General responsibilities of sponsors.
- 21 C.F.R. § 812.42FDA and IRB approval.
- 21 C.F.R. § 812.43Selecting investigators and monitors.
- 21 C.F.R. § 812.45Informing investigators.
- 21 C.F.R. § 812.46Monitoring investigations.
- 21 C.F.R. § 812.47Emergency research under § 50.24 of this chapter.