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.
Title 40 published on 2014-07-01
no entries appear in the Federal Register after this date.