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.

• 5 U.S.C. 301; 7 U.S.C. 136a(a) and 136w(a)(1); 21 U.S.C. 346a(e)(1)(C); sec. 201, Pub. L. 109-54, 119 Stat. 531; and 42 U.S.C. 300v-1(b).
• Source: 56 FR 28012, 28022, June 18, 1991, unless otherwise noted.

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

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