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.