38 CFR Part 16
PROTECTION OF HUMAN SUBJECTS
November 5, 2020
§
16.104
Exempt research
§
§16.105-16.106
[Reserved]
§
16.112
Review by Institution
§
16.101
To what does this policy apply?
§
16.102
Definitions for purposes of this policy
§
16.103
Assuring compliance with this policy—research conducted or supported by any Federal department or agency
§
16.107
IRB membership
§
16.108
IRB functions and operations
§
16.109
IRB review of research
§
16.110
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research
§
16.111
Criteria for IRB approval of research
§
16.113
Suspension or Termination of IRB Approval of Research
§
16.114
Cooperative Research
§
16.115
IRB Records
§
16.116
General Requirements for Informed Consent
§
16.117
Documentation of informed consent
§
16.118
Applications and proposals lacking definite plans for involvement of human subjects
§
16.119
Research undertaken without the intention of involving human subjects
§
16.120
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency
§
16.121
[Reserved]
§
16.122
Use of Federal funds
§
16.123
Early termination of research support: Evaluation of applications and proposals
§
16.124
Conditions
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