Title 40

PART 26 SUBPART K

Subpart K - Basic Ethical Requirements for Third-Party Human Research for Pesticides Involving Intentional Exposure of Non-Pregnant, Non-Nursing Adults Source:84 FR 35318, July 23, 2019, unless otherwise noted.

40:1.0.1.1.25.6.1.1SECTION 26.1101
   26.1101 To what does this subpart apply
40:1.0.1.1.25.6.1.2SECTION 26.1102
   26.1102 Definitions.
40:1.0.1.1.25.6.1.3SECTION 26.1103-26.1106
   26.1103-26.1106 [Reserved]
40:1.0.1.1.25.6.1.4SECTION 26.1107
   26.1107 IRB membership.
40:1.0.1.1.25.6.1.5SECTION 26.1108
   26.1108 IRB functions and operations.
40:1.0.1.1.25.6.1.6SECTION 26.1109
   26.1109 IRB review of research.
40:1.0.1.1.25.6.1.7SECTION 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.
40:1.0.1.1.25.6.1.8SECTION 26.1111
   26.1111 Criteria for IRB approval of research.
40:1.0.1.1.25.6.1.9SECTION 26.1112
   26.1112 Review by institution.
40:1.0.1.1.25.6.1.10SECTION 26.1113
   26.1113 Suspension or termination of IRB approval of research.
40:1.0.1.1.25.6.1.11SECTION 26.1114
   26.1114 Cooperative research.
40:1.0.1.1.25.6.1.12SECTION 26.1115
   26.1115 IRB records.
40:1.0.1.1.25.6.1.13SECTION 26.1116
   26.1116 General requirements for informed consent.
40:1.0.1.1.25.6.1.14SECTION 26.1117
   26.1117 Documentation of informed consent.
40:1.0.1.1.25.6.1.15SECTION 26.1118-26.1122
   26.1118-26.1122 [Reserved]
40:1.0.1.1.25.6.1.16SECTION 26.1123
   26.1123 Early termination of research.
40:1.0.1.1.25.6.1.17SECTION 26.1124
   26.1124 [Reserved]
40:1.0.1.1.25.6.1.18SECTION 26.1125
   26.1125 Prior submission of proposed human research for EPA review.