Subpart A—Federal Policy for the Protection of Human Subjects (Basic ED Policy for Protection of Human Research Subjects)
Sections
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97-97.106
§§ 97-97.106 [Reserved] -
97.101
§ 97.101 To what does this policy apply? -
97.102
§ 97.102 Definitions for purposes of this policy. -
97.103
§ 97.103 Assuring compliance with this policy—research conducted or supported by any Federal department or agency. -
97.104
§ 97.104 Exempt research. -
97.107
§ 97.107 IRB membership. -
97.108
§ 97.108 IRB functions and operations. -
97.109
§ 97.109 IRB review of research. -
97.110
§ 97.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research. -
97.111
§ 97.111 Criteria for IRB approval of research. -
97.112
§ 97.112 Review by Institution -
97.113
§ 97.113 Suspension or Termination of IRB Approval of Research. -
97.114
§ 97.114 Cooperative Research. -
97.115
§ 97.115 IRB Records. -
97.116
§ 97.116 General Requirements for Informed Consent. -
97.117
§ 97.117 Documentation of informed consent. -
97.118
§ 97.118 Applications and proposals lacking definite plans for involvement of human subjects. -
97.119
§ 97.119 Research undertaken without the intention of involving human subjects. -
97.120
§ 97.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency. -
97.121
§ 97.121 [Reserved] -
97.122
§ 97.122 Use of Federal funds. -
97.123
§ 97.123 Early termination of research support: Evaluation of applications and proposals. -
97.124
§ 97.124 Conditions.