Code of Federal Regulations (Last Updated: November 8, 2024) |
Title 16 - Commercial Practices |
Chapter II - Consumer Product Safety Commission |
SubChapter A - General |
Part 1028 - Protection of Human Subjects |
§ 1028.101 - To what does this policy apply? |
§ 1028.102 - Definitions for purposes of this policy. |
§ 1028.103 - Assuring compliance with this policy - research conducted or supported by any Federal Department or Agency. |
§ 1028.104 - Exempt research. |
§ 1028.107 - IRB membership. |
§ 1028.108 - IRB functions and operations. |
§ 1028.109 - IRB review of research. |
§ 1028.110 - Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research. |
§ 1028.111 - Criteria for IRB approval of research. |
§ 1028.112 - Review by institution. |
§ 1028.113 - Suspension or termination of IRB approval of research. |
§ 1028.114 - Cooperative research. |
§ 1028.115 - IRB records. |
§ 1028.116 - General requirements for informed consent. |
§ 1028.117 - Documentation of informed consent. |
§ 1028.118 - Applications and proposals lacking definite plans for involvement of human subjects. |
§ 1028.119 - Research undertaken without the intention of involving human subjects. |
§ 1028.120 - Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency. |
§ 1028.121 - [Reserved] |
§ 1028.122 - Use of Federal funds. |
§ 1028.123 - Early termination of research support: Evaluation of applications and proposals. |
§ 1028.124 - Conditions |
§§ 1028.104--1028.106 - [Reserved] |
§§ 1028.105--1028.106 - [Reserved.] |