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.