Part 16 - Protection of Human Subjects  


§ 16.101 - To what does this policy apply?
§ 16.102 - Definitions for purposes of this policy.
§ 16.103 - Assuring compliance with this policy - research conducted or supported by any Federal Department or Agency.
§ 16.104 - Exempt research.
§ 16.107 - IRB membership.
§ 16.108 - IRB functions and operations.
§ 16.109 - IRB review of research.
§ 16.110 - Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
§ 16.111 - Criteria for IRB approval of research.
§ 16.112 - Review by Institution
§ 16.113 - Suspension or termination of IRB approval of research.
§ 16.114 - Cooperative research.
§ 16.115 - IRB records.
§ 16.116 - General requirements for informed consent.
§ 16.117 - Documentation of informed consent.
§ 16.118 - Applications and proposals lacking definite plans for involvement of human subjects.
§ 16.119 - Research undertaken without the intention of involving human subjects.
§ 16.120 - Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency.
§ 16.121 - [Reserved]
§ 16.122 - Use of Federal funds.
§ 16.123 - Early termination of research support: Evaluation of applications and proposals.
§ 16.124 - Conditions.
§§ 16.104--16.106 - [Reserved]
§§ 16.105--16.106 - [Reserved]