16 CFR Part 1028 — Protection of Human Subjects
- § 1028.101— To what does this policy apply?
- § 1028.102— Definitions for purposes of this policy.
- § 1028.103— Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
- § 1028.104— Exempt research.
- § 1028.107— IRB membership.
- § 1028.108— IRB functions and operations.
- § 1028.109— IRB review of research.
- § 1028.110— Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- § 1028.111— Criteria for IRB approval of research.
- § 1028.112— Review by institution.
- § 1028.113— Suspension or termination of IRB approval of research.
- § 1028.114— Cooperative research.
- § 1028.115— IRB Records.
- § 1028.116— General requirements for informed consent.
- § 1028.117— Documentation of informed consent.
- § 1028.118— Applications and proposals lacking definite plans for involvement of human subjects.
- § 1028.119— Research undertaken without the intention of involving human subjects.
- § 1028.120— Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
- § 1028.122— Use of Federal funds.
- § 1028.123— Early termination of research support: Evaluation of applications and proposals.
- § 1028.124— Conditions