7 CFR Part 1c — Protection of Human Subjects
- § 1c.101— To what does this policy apply?
- § 1c.102— Definitions for purposes of this policy.
- § 1c.103— Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
- § 1c.104— Exempt research.
- § 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.