Title 10, Part 745 — Protection of Human Subjects
23 sections
Section 745.101
To what does this policy apply?
Section 745.102
Definitions for purposes of this policy.
Section 745.103
Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
Section 745.104
Exempt research.
Section 745.105-745.106
§§ 745.105-745.106 [Reserved]
Section 745.107
IRB membership.
Section 745.108
IRB functions and operations.
Section 745.109
IRB review of research.
Section 745.110
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
Section 745.111
Criteria for IRB approval of research.
Section 745.112
Review by Institution
Section 745.113
Suspension or Termination of IRB Approval of Research.
Section 745.114
Cooperative Research.
Section 745.115
IRB Records.
Section 745.116
General Requirements for Informed Consent.
Section 745.117
Documentation of informed consent.
Section 745.118
Applications and proposals lacking definite plans for involvement of human subjects.
Section 745.119
Research undertaken without the intention of involving human subjects.
Section 745.120
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
Section 745.121
[Reserved]
Section 745.122
Use of Federal funds.
Section 745.123
Early termination of research support: Evaluation of applications and proposals.
Section 745.124
Conditions.