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