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U.S. Code of Federal Regulations
Regulations most recently checked for updates: Sep 24, 2023
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Title 21
Chapter I
Part 812
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.
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