16 CFR Part 1028
PART 1028—PROTECTION OF HUMAN SUBJECTS
- PART 1028—PROTECTION OF HUMAN SUBJECTS
- Chapter II—Consumer Product Safety Commission › Subchapter A—General
- § 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
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