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Regulations last checked for updates: Jan 18, 2025
Title 16 - Commercial Practices last revised: Jan 14, 2025
All Titles
Title 16
Chapter II
Part 1028 - PART 1028—PROTECTION OF HUMAN SUBJECTS
§ 1028.101 - To what does this policy apply?
§ 1028.102 - Definitions for purposes of this policy.
§ 1028.103 - Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
§ 1028.104 - Exempt research.
§ 1028.105-1028.106 - [Reserved]
§ 1028.107 - IRB membership.
§ 1028.108 - IRB functions and operations.
§ 1028.109 - IRB review of research.
§ 1028.110 - Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
§ 1028.111 - Criteria for IRB approval of research.
§ 1028.112 - Review by institution.
§ 1028.113 - Suspension or termination of IRB approval of research.
§ 1028.114 - Cooperative research.
§ 1028.115 - IRB Records.
§ 1028.116 - General requirements for informed consent.
§ 1028.117 - Documentation of informed consent.
§ 1028.118 - Applications and proposals lacking definite plans for involvement of human subjects.
§ 1028.119 - Research undertaken without the intention of involving human subjects.
§ 1028.120 - Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
§ 1028.121 - [Reserved]
§ 1028.122 - Use of Federal funds.
§ 1028.123 - Early termination of research support: Evaluation of applications and proposals.
§ 1028.124 - Conditions
authority:
5 U.S.C. 301
;
42 U.S.C. 300v-1
(b)
source:
82 FR 43460, Sept. 18, 2017, unless otherwise noted.
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