PART 16—PROTECTION OF HUMAN SUBJECTS
Sections
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16.101
§ 16.101 To what does this policy apply? -
16.102
§ 16.102 Definitions for purposes of this policy. -
16.103
§ 16.103 Assuring compliance with this policy—research conducted or supported by any Federal department or agency. -
16.104
§ 16.104 Exempt research. -
16.105-16.106
§§ 16.105-16.106 [Reserved] -
16.107
§ 16.107 IRB membership. -
16.108
§ 16.108 IRB functions and operations. -
16.109
§ 16.109 IRB review of research. -
16.110
§ 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
§ 16.111 Criteria for IRB approval of research. -
16.112
§ 16.112 Review by Institution -
16.113
§ 16.113 Suspension or Termination of IRB Approval of Research. -
16.114
§ 16.114 Cooperative Research. -
16.115
§ 16.115 IRB Records. -
16.116
§ 16.116 General Requirements for Informed Consent. -
16.117
§ 16.117 Documentation of informed consent. -
16.118
§ 16.118 Applications and proposals lacking definite plans for involvement of human subjects. -
16.119
§ 16.119 Research undertaken without the intention of involving human subjects. -
16.120
§ 16.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency. -
16.121
§ 16.121 [Reserved] -
16.122
§ 16.122 Use of Federal funds. -
16.123
§ 16.123 Early termination of research support: Evaluation of applications and proposals. -
16.124
§ 16.124 Conditions.