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29 C.F.R. § 21.121
[Reserved]
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Source: 82 FR 7271, Jan. 19, 2017, unless otherwise noted.
Table of Contents
PART 21—PROTECTION OF HUMAN SUBJECTS
- §21.101 To what does this policy apply?
- §21.102 Definitions for purposes of this policy.
- §21.103 Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
- §21.104 Exempt research.
- §21.105-21.106 [Reserved]
- §21.107 IRB membership.
- §21.108 IRB functions and operations.
- §21.109 IRB review of research.
- §21.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- §21.111 Criteria for IRB approval of research.
- §21.112 Review by Institution
- §21.113 Suspension or Termination of IRB Approval of Research.
- §21.114 Cooperative Research.
- §21.115 IRB Records.
- §21.116 General Requirements for Informed Consent.
- §21.117 Documentation of informed consent.
- §21.118 Applications and proposals lacking definite plans for involvement of human subjects.
- §21.119 Research undertaken without the intention of involving human subjects.
- §21.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
- §21.121 [Reserved]
- §21.122 Use of Federal funds.
- §21.123 Early termination of research support: Evaluation of applications and proposals.
- §21.124 Conditions.