PART 1c—PROTECTION OF HUMAN SUBJECTS
- 1c.101—To what does this policy apply?
- 1c.102—Definitions.
- 1c.103—Assuring compliance with this policy—research conducted or supported by any Federal Department or Agency.
- 1c.107—IRB membership.
- 1c.108—IRB functions and operations.
- 1c.109—IRB review of research.
- 1c.110—Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- 1c.111—Criteria for IRB approval of research.
- 1c.112—Review by institution.
- 1c.113—Suspension or termination of IRB approval of research.
- 1c.114—Cooperative research.
- 1c.115—IRB records.
- 1c.116—General requirements for informed consent.
- 1c.117—Documentation of informed consent.
- 1c.118—Applications and proposals lacking definite plans for involvement of human subjects.
- 1c.119—Research undertaken without the intention of involving human subjects.
- 1c.120—Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency.
- 1c.122—Use of Federal funds.
- 1c.123—Early termination of research support: Evaluation of applications and proposals.
- 1c.124—Conditions.