Title 22, Part 225 — Protection of Human Subjects
23 sections
Section 225.101
To what does this policy apply?
Section 225.102
Definitions for purposes of this policy.
Section 225.103
Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
Section 225.104
Exempt research.
Section 225.105-225.106
§§ 225.105-225.106 [Reserved]
Section 225.107
IRB membership.
Section 225.108
IRB functions and operations.
Section 225.109
IRB review of research.
Section 225.110
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
Section 225.111
Criteria for IRB approval of research.
Section 225.112
Review by Institution
Section 225.113
Suspension or Termination of IRB Approval of Research.
Section 225.114
Cooperative Research.
Section 225.115
IRB Records.
Section 225.116
General Requirements for Informed Consent.
Section 225.117
Documentation of informed consent.
Section 225.118
Applications and proposals lacking definite plans for involvement of human subjects.
Section 225.119
Research undertaken without the intention of involving human subjects.
Section 225.120
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
Section 225.121
[Reserved]
Section 225.122
Use of Federal funds.
Section 225.123
Early termination of research support: Evaluation of applications and proposals.
Section 225.124
Conditions.