CFR /  Title 34  /  Part 97: Protection Of Human Subjects

Section No.	Description
Section 97.101	Definitions
Section 97.102	Assuring compliance with this policy--research conducted or supported by any Federal Department or Agency
Section 97.103	IRB membership
Section 97.107	IRB functions and operations
Section 97.108	IRB review of research
Section 97.109	Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes
Section 97.110	Criteria for IRB approval of research
Section 97.111	Review by institution
Section 97.112	Suspension or termination of IRB approval of research
Section 97.113	Cooperative research
Section 97.114	IRB records
Section 97.115	General requirements for informed consent
Section 97.116	Documentation of informed consent
Section 97.117	Applications and proposals lacking definite plans for involvement of human subjects
Section 97.118	Research undertaken without the intention of involving human subjects
Section 97.119	Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department
Section 97.120	Use of Federal funds
Section 97.122	Early termination of research support: Evaluation of applications and proposals
Section 97.123	Conditions
Section 97.124	To what do these regulations apply?
Section 97.401	Definitions
Section 97.402	IRB duties
Section 97.403	Research not involving greater than minimal risk
Section 97.404	Research involving greater than minimal risk but presenting the prospect of direct benefit to the individual subjects
Section 97.405	Research involving greater than minimal risk and no prospect of direct benefit to individual subjects, but likely to
Section 97.406	Research not otherwise approvable which presents an opportunity to understand, prevent, or alleviate a serious
Section 97.407	Requirements for permission by parents or guardians and for assent by children
Section 97.408	Wards
Section 97.409	Applicability of part