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Protection of Human Subjects
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CFR 32
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Protection of Human Subjects
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Section
219.101
To what does this policy apply?
Section
219.102
Definitions for purposes of this policy.
Section
219.103
Assuring compliance with this policy - research conducted or supported by any Federal department or agency.
Section
219.104
Exempt research.
Sections
219.105-219.106
§§ 219.105-219.106 [Reserved]
Section
219.107
IRB membership.
Section
219.108
IRB functions and operations.
Section
219.109
IRB review of research.
Section
219.110
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
Section
219.111
Criteria for IRB approval of research.
Section
219.112
Review by Institution
Section
219.113
Suspension or Termination of IRB Approval of Research.
Section
219.114
Cooperative Research.
Section
219.115
IRB Records.
Section
219.116
General Requirements for Informed Consent.
Section
219.117
Documentation of informed consent.
Section
219.118
Applications and proposals lacking definite plans for involvement of human subjects.
Section
219.119
Research undertaken without the intention of involving human subjects.
Section
219.120
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
Section
219.121
§ 219.121 [Reserved]
Section
219.122
Use of Federal funds.
Section
219.123
Early termination of research support: Evaluation of applications and proposals.
Section
219.124
Conditions.