Code of Federal Regulations (Last Updated: November 8, 2024) |
Title 45 - Public Welfare |
Subtitle A - Department of Health and Human Services |
SubChapter A - General Administration |
Part 46 - Protection of Human Subjects |
Subpart A - Basic HHS Policy for Protection of Human Research Subjects |
§ 46.101 - To what does this policy apply? |
§ 46.102 - Definitions for purposes of this policy. |
§ 46.103 - Assuring compliance with this policy - research conducted or supported by any Federal Department or Agency. |
§ 46.104 - Exempt research. |
§ 46.107 - IRB membership. |
§ 46.108 - IRB functions and operations. |
§ 46.109 - IRB review of research. |
§ 46.110 - Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research. |
§ 46.111 - Criteria for IRB approval of research. |
§ 46.112 - Review by institution. |
§ 46.113 - Suspension or termination of IRB approval of research. |
§ 46.114 - Cooperative research. |
§ 46.115 - IRB records. |
§ 46.116 - General requirements for informed consent. |
§ 46.117 - Documentation of informed consent. |
§ 46.118 - Applications and proposals lacking definite plans for involvement of human subjects. |
§ 46.119 - Research undertaken without the intention of involving human subjects. |
§ 46.120 - Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency. |
§ 46.121 - [Reserved] |
§ 46.122 - Use of Federal funds. |
§ 46.123 - Early termination of research support: Evaluation of applications and proposals. |
§ 46.124 - Conditions. |
§§ 46.104--46.106 - [Reserved] |
§§ 46.105--46.106 - [Reserved] |