Title 32, Part 219 — Protection of Human Subjects
23 sections
Section 219.101
To what does this policy apply?
Section 219.102
Definitions for purposes of this policy.
Section 219.103
Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
Section 219.104
Exempt research.
Section 219.105-219.106
§§ 219.105-219.106 [Reserved]
Section 219.107
IRB membership.
Section 219.108
IRB functions and operations.
Section 219.109
IRB review of research.
Section 219.110
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
Section 219.111
Criteria for IRB approval of research.
Section 219.112
Review by Institution
Section 219.113
Suspension or Termination of IRB Approval of Research.
Section 219.114
Cooperative Research.
Section 219.115
IRB Records.
Section 219.116
General Requirements for Informed Consent.
Section 219.117
Documentation of informed consent.
Section 219.118
Applications and proposals lacking definite plans for involvement of human subjects.
Section 219.119
Research undertaken without the intention of involving human subjects.
Section 219.120
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
Section 219.121
[Reserved]
Section 219.122
Use of Federal funds.
Section 219.123
Early termination of research support: Evaluation of applications and proposals.
Section 219.124
Conditions.