Part 21. PART 21—PROTECTION OF HUMAN SUBJECTS
- § 21.101 - To what does this policy apply?
- § 21.102 - Definitions for purposes of this policy.
- § 21.103 - Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
- § 21.104 - Exempt research.
- §§ 21.105-21.106 - §[Reserved]
- § 21.107 - IRB membership.
- § 21.108 - IRB functions and operations.
- § 21.109 - IRB review of research.
- § 21.110 - Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- § 21.111 - Criteria for IRB approval of research.
- § 21.112 - Review by Institution
- § 21.113 - Suspension or Termination of IRB Approval of Research.
- § 21.114 - Cooperative Research.
- § 21.115 - IRB Records.
- § 21.116 - General Requirements for Informed Consent.
- § 21.117 - Documentation of informed consent.
- § 21.118 - Applications and proposals lacking definite plans for involvement of human subjects.
- § 21.119 - Research undertaken without the intention of involving human subjects.
- § 21.120 - Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
- § 21.121 - [Reserved]
- § 21.122 - Use of Federal funds.
- § 21.123 - Early termination of research support: Evaluation of applications and proposals.
- § 21.124 - Conditions.