SUBPART C—Responsibilities of Sponsors (§812.40 to §812.47)
- 812.40—General responsibilities of sponsors.
- 812.42—FDA and IRB approval.
- 812.43—Selecting investigators and monitors.
- 812.45—Informing investigators.
- 812.46—Monitoring investigations.
- 812.47—Emergency research under § 50.24 of this chapter.