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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 40 - Protection of Environment |
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Chapter I - Environmental Protection Agency |
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SubChapter A - General |
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Part 26 - Protection of Human Subjects |
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Subpart K - Basic Ethical Requirements for Third-Party Human Research for Pesticides Involving Intentional Exposure of Non-pregnant, Non-nursing Adults |
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. |
| § 26.1107 - 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. |
| § 26.1123 - Early termination of research. |
| § 26.1124 - [Reserved] |
| § 26.1125 - Prior submission of proposed human research for EPA review. |
| §§ 26.1103--26.1106 - [Reserved] |
| §§ 26.1118--26.1122 - [Reserved] |