Subpart B—Informed Consent of Human Subjects

1. CFR
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3. Title 21
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5. Chapter I
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7. Part 50
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9. Subpart B

Sections

Section numbering in the official eCFR can be non-consecutive. Omitted section numbers are not treated here as reserved unless the source explicitly labels them that way.

• 50.20
  § 50.20 General requirements for informed consent.
• 50.22
  § 50.22 Exception from informed consent requirements for minimal risk clinical investigations.
• 50.23
  § 50.23 Exception from general requirements.
• 50.24
  § 50.24 Exception from informed consent requirements for emergency research.
• 50.25
  § 50.25 Elements of informed consent.
• 50.27
  § 50.27 Documentation of informed consent.