REGULATIONS
Rulings
AD/CVD
Notices
HTSUS
U.S. Code
Regs
More
Ports
About
Updates
Apps
Larger font
Smaller font
SEARCH
Sort by Rank
Titles Ascending
Titles Descending
10 per page
25 Result/page
50 Result/page
Regulations last checked for updates: May 22, 2025
Title 21 - Food and Drugs last revised: May 19, 2025
All Titles
Title 21
Chapter I
Part 50
Subpart B - Subpart B—Informed Consent of Human Subjects
§ 50.20 - General requirements for informed consent.
§ 50.22 - Exception from informed consent requirements for minimal risk clinical investigations.
§ 50.23 - Exception from general requirements.
§ 50.24 - Exception from informed consent requirements for emergency research.
§ 50.25 - Elements of informed consent.
§ 50.27 - Documentation of informed consent.
authority:
21 U.S.C. 321
,
343
,
346
,
346
a,
348
,
350a
,
350b
,
352
,
353
,
355
,
360
,
360
c-360f,
360
h-360j,
371
,
379e
,
381
;
42 U.S.C. 216
,
241
,
262
source:
45 FR 36390, May 30, 1980, unless otherwise noted.
.list_box li,p,.cm-search-info,.cm-search-detail,.abt span,.expand-collapse_top
Get the CustomsMobile app!