Part 431—Protection of Human Subjects

1. CFR
2. ›
3. Title 20
4. ›
5. Chapter III
6. ›
7. Part 431

Sections

• 431.101
  § 431.101 To what does this policy apply?
• 431.102
  § 431.102 Definitions for purposes of this policy.
• 431.103
  § 431.103 Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
• 431.104
  § 431.104 Exempt research.
• 431.105-431.106
  §§ 431.105-431.106 [Reserved]
• 431.107
  § 431.107 IRB membership.
• 431.108
  § 431.108 IRB functions and operations.
• 431.109
  § 431.109 IRB review of research.
• 431.110
  § 431.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
• 431.111
  § 431.111 Criteria for IRB approval of research.
• 431.112
  § 431.112 Review by Institution
• 431.113
  § 431.113 Suspension or Termination of IRB Approval of Research.
• 431.114
  § 431.114 Cooperative Research.
• 431.115
  § 431.115 IRB Records.
• 431.116
  § 431.116 General Requirements for Informed Consent.
• 431.117
  § 431.117 Documentation of informed consent.
• 431.118
  § 431.118 Applications and proposals lacking definite plans for involvement of human subjects.
• 431.119
  § 431.119 Research undertaken without the intention of involving human subjects.
• 431.120
  § 431.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
• 431.121
  § 431.121 [Reserved]
• 431.122
  § 431.122 Use of Federal funds.
• 431.123
  § 431.123 Early termination of research support: Evaluation of applications and proposals.
• 431.124
  § 431.124 Conditions.