Title 20, Part 431 — Protection of Human Subjects
23 sections
Section 431.101
To what does this policy apply?
Section 431.102
Definitions for purposes of this policy.
Section 431.103
Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
Section 431.104
Exempt research.
Section 431.105-431.106
§§ 431.105-431.106 [Reserved]
Section 431.107
IRB membership.
Section 431.108
IRB functions and operations.
Section 431.109
IRB review of research.
Section 431.110
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
Section 431.111
Criteria for IRB approval of research.
Section 431.112
Review by Institution
Section 431.113
Suspension or Termination of IRB Approval of Research.
Section 431.114
Cooperative Research.
Section 431.115
IRB Records.
Section 431.116
General Requirements for Informed Consent.
Section 431.117
Documentation of informed consent.
Section 431.118
Applications and proposals lacking definite plans for involvement of human subjects.
Section 431.119
Research undertaken without the intention of involving human subjects.
Section 431.120
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
Section 431.121
[Reserved]
Section 431.122
Use of Federal funds.
Section 431.123
Early termination of research support: Evaluation of applications and proposals.
Section 431.124
Conditions.