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Protection of Human Subjects
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Section
1c.101
To what does this policy apply?
Section
1c.102
Definitions for purposes of this policy.
Section
1c.103
Assuring compliance with this policy - research conducted or supported by any Federal department or agency.
Section
1c.104
Exempt research.
Sections
1c.105-1c.106
§§ 1c.105-1c.106 [Reserved]
Section
1c.107
IRB membership.
Section
1c.108
IRB functions and operations.
Section
1c.109
IRB review of research.
Section
1c.110
Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
Section
1c.111
Criteria for IRB approval of research.
Section
1c.112
Review by Institution
Section
1c.113
Suspension or Termination of IRB Approval of Research.
Section
1c.114
Cooperative Research.
Section
1c.115
IRB Records.
Section
1c.116
General Requirements for Informed Consent.
Section
1c.117
Documentation of informed consent.
Section
1c.118
Applications and proposals lacking definite plans for involvement of human subjects.
Section
1c.119
Research undertaken without the intention of involving human subjects.
Section
1c.120
Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
Section
1c.121
§ 1c.121 [Reserved]
Section
1c.122
Use of Federal funds.
Section
1c.123
Early termination of research support: Evaluation of applications and proposals.
Section
1c.124
Conditions.