Part 16. 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.
- §§ 16.105-16.106 - §[Reserved]
- § 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.