Part 219 — Protection of Human Subjects
- §219.101 To what does this policy apply?
- §219.102 Definitions for purposes of this policy.
- §219.103 Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
- §219.104 Exempt research.
- §219.105-219.106 Reserved
- §219.107 IRB membership.
- §219.108 IRB functions and operations.
- §219.109 IRB review of research.
- §219.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- §219.111 Criteria for IRB approval of research.
- §219.112 Review by Institution
- §219.113 Suspension or Termination of IRB Approval of Research.
- §219.114 Cooperative Research.
- §219.115 IRB Records.
- §219.116 General Requirements for Informed Consent.
- §219.117 Documentation of informed consent.
- §219.118 Applications and proposals lacking definite plans for involvement of human subjects.
- §219.119 Research undertaken without the intention of involving human subjects.
- §219.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
- §219.121 Reserved
- §219.122 Use of Federal funds.
- §219.123 Early termination of research support: Evaluation of applications and proposals.
- §219.124 Conditions.