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Section 1c.101
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Definitions |
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Section 1c.102
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Assuring compliance with this policy--research conducted or supported by any Federal Department or Agency |
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Section 1c.103
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IRB membership |
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Section 1c.107
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IRB functions and operations |
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Section 1c.108
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IRB review of research |
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Section 1c.109
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Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved |
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Section 1c.110
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Criteria for IRB approval of research |
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Section 1c.111
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Review by institution |
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Section 1c.112
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Suspension or termination of IRB approval of research |
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Section 1c.113
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Cooperative research |
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Section 1c.114
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IRB records |
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Section 1c.115
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General requirements for informed consent |
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Section 1c.116
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Documentation of informed consent |
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Section 1c.117
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Applications and proposals lacking definite plans for involvement of human subjects |
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Section 1c.118
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Research undertaken without the intention of involving human subjects |
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Section 1c.119
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Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department |
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Section 1c.120
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Use of Federal funds |
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Section 1c.122
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Early termination of research support: Evaluation of applications and proposals |
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Section 1c.123
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Conditions |
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Section 1c.124
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Establishment of the Department |