21 CFR Subpart B - Subpart B—Informed Consent of Human Subjects
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- § 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.
Source:
46 FR 8951, Jan. 27, 1981, unless otherwise noted.