Part 16 - PROTECTION OF HUMAN SUBJECTS
- Section 16.101 - To what does this policy apply?
- Section 16.102 - Definitions for purposes of this policy
- Section 16.103 - Assuring compliance with this policy-research conducted or supported by any Federal department or agency
- Section 16.104 - Exempt research
- Section 16.105-16.106 - Reserved
- Section 16.107 - IRB membership
- Section 16.108 - IRB functions and operations
- Section 16.109 - IRB review of research
- Section 16.110 - Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research
- Section 16.111 - Criteria for IRB approval of research
- Section 16.112 - Review by Institution
- Section 16.113 - Suspension or Termination of IRB Approval of Research
- Section 16.114 - Cooperative Research
- Section 16.115 - IRB Records
- Section 16.116 - General Requirements for Informed Consent
- Section 16.117 - Documentation of informed consent
- Section 16.118 - Applications and proposals lacking definite plans for involvement of human subjects
- Section 16.119 - Research undertaken without the intention of involving human subjects
- Section 16.120 - Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency
- Section 16.121 - Reserved
- Section 16.122 - Use of Federal funds
- Section 16.123 - Early termination of research support: Evaluation of applications and proposals
- Section 16.124 - Conditions