Code of Federal Regulations (alpha)

CFR /  Title 38  /  Part 16: Protection Of Human Subjects

Section No. Description
Section 16.101 Definitions
Section 16.102 Assuring compliance with this policy--research conducted or supported by any Federal Department or Agency
Section 16.103 IRB membership
Section 16.107 IRB functions and operations
Section 16.108 IRB review of research
Section 16.109 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor
Section 16.110 Criteria for IRB approval of research
Section 16.111 Review by institution
Section 16.112 Suspension or termination of IRB approval of research
Section 16.113 Cooperative research
Section 16.114 IRB records
Section 16.115 General requirements for informed consent
Section 16.116 Documentation of informed consent
Section 16.117 Applications and proposals lacking definite plans for involvement of human subjects
Section 16.118 Research undertaken without the intention of involving human subjects
Section 16.119 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or
Section 16.120 Use of Federal funds
Section 16.122 Early termination of research support: Evaluation of applications and proposals
Section 16.123 Conditions
Section 16.124 Incorporation by reference