Subpart C. Subpart C—Responsibilities of Sponsors

• § 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 of this chapter.