PART 431—PROTECTION OF HUMAN SUBJECTS
Table of Contents
Sec. | |
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431.101 | To what does this policy apply? |
431.102 | Definitions for purposes of this policy. |
431.103 | Assuring compliance with this policy—research conducted or supported by any Federal department or agency. |
431.104 | Exempt research. |
431.105–431.106 | [Reserved] |
431.107 | IRB membership. |
431.108 | IRB functions and operations. |
431.109 | IRB review of research. |
431.110 | Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research. |
431.111 | Criteria for IRB approval of research. |
431.112 | Review by institution. |
431.113 | Suspension or termination of IRB approval of research. |
431.114 | Cooperative research. |
431.115 | IRB records. |
431.116 | General requirements for informed consent. |
431.117 | Documentation of informed consent. |
431.118 | Applications and proposals lacking definite plans for involvement of human subjects. |
431.119 | Research undertaken without the intention of involving human subjects. |
431.120 | Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency. |
431.121 | [Reserved] |
431.122 | Use of Federal funds. |
431.123 | Early termination of research support: Evaluation of applications and proposals. |
431.124 | Conditions. |
Authority: 5 U.S.C. 301; 42 U.S.C. 289(a).
Source: 82 FR 7270, Jan. 19, 2017, unless otherwise noted.