Code of Federal Regulations > Title 40 > Chapter I > 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

U.S. Code of Federal Regulations

Regulations most recently checked for updates: Aug 27, 2025

§ 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.