PART 16—PROTECTION OF HUMAN SUBJECTS
- 16.101—To what does this policy apply?
- 16.102—Definitions.
- 16.103—Assuring compliance with this policy—research conducted or supported by any Federal Department or Agency.
- 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.
- 16.122—Use of Federal funds.
- 16.123—Early termination of research support: Evaluation of applications and proposals.
- 16.124—Conditions.