7 CFR Part 1c - PROTECTION OF HUMAN SUBJECTS
- § 1c.101 — To what does this policy apply?
- § 1c.102 — Definitions.
- § 1c.103 — Assuring compliance with this policy—research conducted or supported by any Federal Department or Agency.
- §§ 1c.104-1c.106 — [Reserved]
- § 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.121 — [Reserved]
- § 1c.122 — Use of Federal funds.
- § 1c.123 — Early termination of research support: Evaluation of applications and proposals.
- § 1c.124 — Conditions.
Authority:
Source:
56 FR 28012, 28018, June 18, 1991, unless otherwise noted.
Title 7 published on 2013-01-01
no entries appear in the Federal Register after this date.
