Federal (United States) · Regulations
Subpart B
6 sections
6 sections
- 21 C.F.R. § 50.20General requirements for informed consent.
- 21 C.F.R. § 50.22Exception from informed consent requirements for minimal risk clinical investigations.
- 21 C.F.R. § 50.23Exception from general requirements.
- 21 C.F.R. § 50.24Exception from informed consent requirements for emergency research.
- 21 C.F.R. § 50.25Elements of informed consent.
- 21 C.F.R. § 50.27Documentation of informed consent.