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Title 16
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Part 1028
FEDERAL · 16 CFR
Part 1028 — Protection of Human Subjects
23 sections · Title 16: Commercial Practices
§ 1028.101
To what does this policy apply?
§ 1028.102
Definitions for purposes of this policy.
§ 1028.103
Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
§ 1028.104
Exempt research.
§ 1028.105-1028.106
§ 1028.105-1028.106 [Reserved]
§ 1028.107
IRB membership.
§ 1028.108
IRB functions and operations.
§ 1028.109
IRB review of research.
§ 1028.110
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
§ 1028.111
Criteria for IRB approval of research.
§ 1028.112
Review by institution.
§ 1028.113
Suspension or termination of IRB approval of research.
§ 1028.114
Cooperative research.
§ 1028.115
IRB Records.
§ 1028.116
General requirements for informed consent.
§ 1028.117
Documentation of informed consent.
§ 1028.118
Applications and proposals lacking definite plans for involvement of human subjects.
§ 1028.119
Research undertaken without the intention of involving human subjects.
§ 1028.120
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
§ 1028.121
§ 1028.121 [Reserved]
§ 1028.122
Use of Federal funds.
§ 1028.123
Early termination of research support: Evaluation of applications and proposals.
§ 1028.124
Conditions