40 CFR Part 26, Subpart K - Basic Ethical Requirements for Third-Party Human Research for Pesticides Involving Intentional Exposure of Non-pregnant, Non-nursing Adults
- § 26.1101 To what does this subpart apply?
- § 26.1102 Definitions.
- §§ 26.1103-26.1106 [Reserved]
- § 26.1107 IRB membership.
- § 26.1108 IRB functions and operations.
- § 26.1109 IRB review of research.
- § 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 Criteria for IRB approval of research.
- § 26.1112 Review by institution.
- § 26.1113 Suspension or termination of IRB approval of research.
- § 26.1114 Cooperative research.
- § 26.1115 IRB records.
- § 26.1116 General requirements for informed consent.
- § 26.1117 Documentation of informed consent.
- §§ 26.1118-26.1122 [Reserved]
- § 26.1123 Early termination of research.
- § 26.1124 [Reserved]
- § 26.1125 Prior submission of proposed human research for EPA review.
Source:
71 FR 6168, Feb. 6, 2006, unless otherwise noted.