10 CFR Part 745 — Protection of Human Subjects
- § 745.101— To what does this policy apply?
- § 745.102— Definitions for purposes of this policy.
- § 745.103— Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
- § 745.104— Exempt research.
- § 745.107— IRB membership.
- § 745.108— IRB functions and operations.
- § 745.109— IRB review of research.
- § 745.110— Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- § 745.111— Criteria for IRB approval of research.
- § 745.112— Review by Institution
- § 745.113— Suspension or Termination of IRB Approval of Research.
- § 745.114— Cooperative Research.
- § 745.115— IRB Records.
- § 745.116— General Requirements for Informed Consent.
- § 745.117— Documentation of informed consent.
- § 745.118— Applications and proposals lacking definite plans for involvement of human subjects.
- § 745.119— Research undertaken without the intention of involving human subjects.
- § 745.120— Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
- § 745.122— Use of Federal funds.
- § 745.123— Early termination of research support: Evaluation of applications and proposals.
- § 745.124— Conditions.