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