Part 219—Protection of Human Subjects

1. CFR
2. ›
3. Title 32
4. ›
5. Subtitle A
6. ›
7. Chapter I
8. ›
9. Part 219

Sections

• 219.101
  § 219.101 To what does this policy apply?
• 219.102
  § 219.102 Definitions for purposes of this policy.
• 219.103
  § 219.103 Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
• 219.104
  § 219.104 Exempt research.
• 219.105-219.106
  §§ 219.105-219.106 [Reserved]
• 219.107
  § 219.107 IRB membership.
• 219.108
  § 219.108 IRB functions and operations.
• 219.109
  § 219.109 IRB review of research.
• 219.110
  § 219.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
• 219.111
  § 219.111 Criteria for IRB approval of research.
• 219.112
  § 219.112 Review by Institution
• 219.113
  § 219.113 Suspension or Termination of IRB Approval of Research.
• 219.114
  § 219.114 Cooperative Research.
• 219.115
  § 219.115 IRB Records.
• 219.116
  § 219.116 General Requirements for Informed Consent.
• 219.117
  § 219.117 Documentation of informed consent.
• 219.118
  § 219.118 Applications and proposals lacking definite plans for involvement of human subjects.
• 219.119
  § 219.119 Research undertaken without the intention of involving human subjects.
• 219.120
  § 219.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
• 219.121
  § 219.121 [Reserved]
• 219.122
  § 219.122 Use of Federal funds.
• 219.123
  § 219.123 Early termination of research support: Evaluation of applications and proposals.
• 219.124
  § 219.124 Conditions.