Subpart A. Subpart A—Basic HHS Policy for Protection of Human Research Subjects
- § 46.101 - To what does this policy apply?
- § 46.102 - Definitions for purposes of this policy.
- § 46.103 - Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
- § 46.104 - Exempt research.
- § 46.105-46.106 - [Reserved]
- § 46.107 - IRB membership.
- § 46.108 - IRB functions and operations.
- § 46.109 - IRB review of research.
- § 46.110 - Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- § 46.111 - Criteria for IRB approval of research.
- § 46.112 - Review by institution.
- § 46.113 - Suspension or termination of IRB approval of research.
- § 46.114 - Cooperative research.
- § 46.115 - IRB records.
- § 46.116 - General requirements for informed consent.
- § 46.117 - Documentation of informed consent.
- § 46.118 - Applications and proposals lacking definite plans for involvement of human subjects.
- § 46.119 - Research undertaken without the intention of involving human subjects.
- § 46.120 - Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
- § 46.121 - [Reserved]
- § 46.122 - Use of Federal funds.
- § 46.123 - Early termination of research support: Evaluation of applications and proposals.
- § 46.124 - Conditions.