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