Federal (United States) · Regulations
Subpart K — Basic Ethical Requirements for Third-Party Human Research for Pesticides Involving Intentional Exposure of Non-Pregnant, Non-Nursing Adults
15 sections
15 sections
- 40 C.F.R. § 26.1101To what does this subpart apply?
- 40 C.F.R. § 26.1102Definitions.
- 40 C.F.R. § 26.1107IRB membership.
- 40 C.F.R. § 26.1108IRB functions and operations.
- 40 C.F.R. § 26.1109IRB review of research.
- 40 C.F.R. § 26.1110Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- 40 C.F.R. § 26.1111Criteria for IRB approval of research.
- 40 C.F.R. § 26.1112Review by institution.
- 40 C.F.R. § 26.1113Suspension or termination of IRB approval of research.
- 40 C.F.R. § 26.1114Cooperative research.
- 40 C.F.R. § 26.1115IRB records.
- 40 C.F.R. § 26.1116General requirements for informed consent.
- 40 C.F.R. § 26.1117Documentation of informed consent.
- 40 C.F.R. § 26.1123Early termination of research.
- 40 C.F.R. § 26.1125Prior submission of proposed human research for EPA review.