10 CFR Part 745 - PROTECTION OF HUMAN SUBJECTS
- § 745.101 To what does this policy apply?
- § 745.102 Definitions.
- § 745.103 Assuring compliance with this policy - research conducted or supported by any Federal department or agency.
- §§ 745.104-745.106 [Reserved]
- § 745.107 IRB membership.
- § 745.108 IRB functions and operations.
- § 745.109 IRB review of research.
- § 745.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- § 745.111 Criteria for IRB approval of research.
- § 745.112 Review by institution.
- § 745.113 Suspension or termination of IRB approval of research.
- § 745.114 Cooperative research.
- § 745.115 IRB records.
- § 745.116 General requirements for informed consent.
- § 745.117 Documentation of informed consent.
- § 745.118 Applications and proposals lacking definite plans for involvement of human subjects.
- § 745.119 Research undertaken without the intention of involving human subjects.
- § 745.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
- § 745.121 [Reserved]
- § 745.122 Use of Federal funds.
- § 745.123 Early termination of research support: Evaluation of applications and proposals.
- § 745.124 Conditions.
Link to an amendment published at 82 FR 7269, Jan. 19, 2017.
Authority:
Source:
56 FR 28012, 28018, June 18, 1991, unless otherwise noted.