Part 21—Protection of Human Subjects

1. CFR
2. ›
3. Title 29
4. ›
5. Subtitle A
6. ›
7. Part 21

Sections

• 21.101
  § 21.101 To what does this policy apply?
• 21.102
  § 21.102 Definitions for purposes of this policy.
• 21.103
  § 21.103 Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
• 21.104
  § 21.104 Exempt research.
• 21.105-21.106
  §§ 21.105-21.106 [Reserved]
• 21.107
  § 21.107 IRB membership.
• 21.108
  § 21.108 IRB functions and operations.
• 21.109
  § 21.109 IRB review of research.
• 21.110
  § 21.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
• 21.111
  § 21.111 Criteria for IRB approval of research.
• 21.112
  § 21.112 Review by Institution
• 21.113
  § 21.113 Suspension or Termination of IRB Approval of Research.
• 21.114
  § 21.114 Cooperative Research.
• 21.115
  § 21.115 IRB Records.
• 21.116
  § 21.116 General Requirements for Informed Consent.
• 21.117
  § 21.117 Documentation of informed consent.
• 21.118
  § 21.118 Applications and proposals lacking definite plans for involvement of human subjects.
• 21.119
  § 21.119 Research undertaken without the intention of involving human subjects.
• 21.120
  § 21.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
• 21.121
  § 21.121 [Reserved]
• 21.122
  § 21.122 Use of Federal funds.
• 21.123
  § 21.123 Early termination of research support: Evaluation of applications and proposals.
• 21.124
  § 21.124 Conditions.