Code of Federal Regulations > Title 34 > Part 97 > Subpart A - Subpart A—Federal Policy for the Protection of Human Subjects (Basic ED Policy for Protection of Human Research Subjects)

U.S. Code of Federal Regulations

Regulations most recently checked for updates: Feb 11, 2026

§ 97.101 - To what does this policy apply?

§ 97.102 - Definitions for purposes of this policy.

§ 97.103 - Assuring compliance with this policy—research conducted or supported by any Federal department or agency.

§§ 97-97.106 - §[Reserved]

§ 97.107 - IRB membership.

§ 97.108 - IRB functions and operations.

§ 97.109 - IRB review of research.

§ 97.110 - Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.

§ 97.111 - Criteria for IRB approval of research.

§ 97.112 - Review by Institution

§ 97.113 - Suspension or Termination of IRB Approval of Research.

§ 97.114 - Cooperative Research.

§ 97.115 - IRB Records.

§ 97.116 - General Requirements for Informed Consent.

§ 97.117 - Documentation of informed consent.

§ 97.118 - Applications and proposals lacking definite plans for involvement of human subjects.

§ 97.119 - Research undertaken without the intention of involving human subjects.

§ 97.120 - Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.

§ 97.121 - [Reserved]

§ 97.122 - Use of Federal funds.

§ 97.123 - Early termination of research support: Evaluation of applications and proposals.

§ 97.124 - Conditions.