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Regulations last checked for updates: May 23, 2025
Title 21 - Food and Drugs last revised: May 19, 2025
All Titles
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.
authority:
21 U.S.C. 331
,
351
,
352
,
353
,
355
,
360
,
360
c-360f,
360
h-360j,
360
hh-360pp,
360
rr-360ss,
360
bbb-8b,
371
,
372
,
374
,
379e
,
381
,
382
;
42 U.S.C. 216
,
241
,
262
source:
45 FR 3751, Jan. 18, 1980, unless otherwise noted.
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