Part 27 — Protection of Human Subjects
- §27.101 To what does this policy apply?
- §27.102 Definitions for purposes of this policy.
- §27.103 Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
- §27.104 Exempt research.
- §27.105-27.106 Reserved
- §27.107 IRB membership.
- §27.108 IRB functions and operations.
- §27.109 IRB review of research.
- §27.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- §27.111 Criteria for IRB approval of research.
- §27.112 Review by Institution
- §27.113 Suspension or Termination of IRB Approval of Research.
- §27.114 Cooperative Research.
- §27.115 IRB Records.
- §27.116 General Requirements for Informed Consent.
- §27.117 Documentation of informed consent.
- §27.118 Applications and proposals lacking definite plans for involvement of human subjects.
- §27.119 Research undertaken without the intention of involving human subjects.
- §27.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
- §27.121 Reserved
- §27.122 Use of Federal funds.
- §27.123 Early termination of research support: Evaluation of applications and proposals.
- §27.124 Conditions.