Code of Federal Regulations · Subpart
Subpart B — Informed Consent Of Human Subjects
21 C.F.R. pt. 50, subpt. B
- § 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