Subpart K—Basic Ethical Requirements for Third-Party Human Research for Pesticides Involving Intentional Exposure of Non-Pregnant, Non-Nursing Adults
Sections
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26.1101
§ 26.1101 To what does this subpart apply? -
26.1102
§ 26.1102 Definitions. -
26.1103-26.1106
§§ 26.1103-26.1106 [Reserved] -
26.1107
§ 26.1107 IRB membership. -
26.1108
§ 26.1108 IRB functions and operations. -
26.1109
§ 26.1109 IRB review of research. -
26.1110
§ 26.1110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research. -
26.1111
§ 26.1111 Criteria for IRB approval of research. -
26.1112
§ 26.1112 Review by institution. -
26.1113
§ 26.1113 Suspension or termination of IRB approval of research. -
26.1114
§ 26.1114 Cooperative research. -
26.1115
§ 26.1115 IRB records. -
26.1116
§ 26.1116 General requirements for informed consent. -
26.1117
§ 26.1117 Documentation of informed consent. -
26.1118-26.1122
§§ 26.1118-26.1122 [Reserved] -
26.1123
§ 26.1123 Early termination of research. -
26.1124
§ 26.1124 [Reserved] -
26.1125
§ 26.1125 Prior submission of proposed human research for EPA review.