38 CFR Part 16 - PROTECTION OF HUMAN SUBJECTS
- § 16.101 — To what does this policy apply?
- § 16.102 — Definitions.
- § 16.103 — Assuring compliance with this policy—research conducted or supported by any Federal Department or Agency.
- §§ 16.104-16.106 — [Reserved]
- § 16.107 — IRB membership.
- § 16.108 — IRB functions and operations.
- § 16.109 — IRB review of research.
- § 16.110 — Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- § 16.111 — Criteria for IRB approval of research.
- § 16.112 — Review by institution.
- § 16.113 — Suspension or termination of IRB approval of research.
- § 16.114 — Cooperative research.
- § 16.115 — IRB records.
- § 16.116 — General requirements for informed consent.
- § 16.117 — Documentation of informed consent.
- § 16.118 — Applications and proposals lacking definite plans for involvement of human subjects.
- § 16.119 — Research undertaken without the intention of involving human subjects.
- § 16.120 — Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency.
- § 16.121 — [Reserved]
- § 16.122 — Use of Federal funds.
- § 16.123 — Early termination of research support: Evaluation of applications and proposals.
- § 16.124 — Conditions.
Authority:
Source:
56 FR 28012, 28021, June 18, 1991, unless otherwise noted.
Title 38 published on 2012-07-01
no entries appear in the Federal Register after this date.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.
