Part 11 — Protection of Human Subjects
- § 11.101— To what does this policy apply?
- § 11.102— Definitions for purposes of this policy.
- § 11.103— Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
- § 11.104— Exempt research.
- § 11.107— IRB membership.
- § 11.108— IRB functions and operations.
- § 11.109— IRB review of research.
- § 11.110— Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- § 11.111— Criteria for IRB approval of research.
- § 11.112— Review by Institution
- § 11.113— Suspension or Termination of IRB Approval of Research.
- § 11.114— Cooperative Research.
- § 11.115— IRB Records.
- § 11.116— General Requirements for Informed Consent.
- § 11.117— Documentation of informed consent.
- § 11.118— Applications and proposals lacking definite plans for involvement of human subjects.
- § 11.119— Research undertaken without the intention of involving human subjects.
- § 11.120— Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
- § 11.122— Use of Federal funds.
- § 11.123— Early termination of research support: Evaluation of applications and proposals.
- § 11.124— Conditions.