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Code of Federal Regulations
Title 38
Chapter I
Part 16
38 C.F.R. Part 16
Protection of Human Subjects
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16.101
To what does this policy apply?
16.102
Definitions for purposes of this policy.
16.103
Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
16.104
Exempt research.
16.105-16.106
[Reserved]
16.107
IRB membership.
16.108
IRB functions and operations.
16.109
IRB review of research.
16.110
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
16.111
Criteria for IRB approval of research.
16.112
Review by Institution
16.113
Suspension or Termination of IRB Approval of Research.
16.114
Cooperative Research.
16.115
IRB Records.
16.116
General Requirements for Informed Consent.
16.117
Documentation of informed consent.
16.118
Applications and proposals lacking definite plans for involvement of human subjects.
16.119
Research undertaken without the intention of involving human subjects.
16.120
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
16.121
[Reserved]
16.122
Use of Federal funds.
16.123
Early termination of research support: Evaluation of applications and proposals.
16.124
Conditions.
16.104-16.106
[Reserved]
Repealed