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45 C.F.R. § 46.121
[Reserved]
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Source: 82 FR 7259, 7273, Jan. 19, 2017, unless otherwise noted.
Table of Contents
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.