Part 1028 - PROTECTION OF HUMAN SUBJECTS
- Section 1028.101 - To what does this policy apply?
- Section 1028.102 - Definitions for purposes of this policy
- Section 1028.103 - Assuring compliance with this policy-research conducted or supported by any Federal department or agency
- Section 1028.104 - Exempt research
- Section 1028.105-1028.106 - Reserved
- Section 1028.107 - IRB membership
- Section 1028.108 - IRB functions and operations
- Section 1028.109 - IRB review of research
- Section 1028.110 - Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research
- Section 1028.111 - Criteria for IRB approval of research
- Section 1028.112 - Review by institution
- Section 1028.113 - Suspension or termination of IRB approval of research
- Section 1028.114 - Cooperative research
- Section 1028.115 - IRB Records
- Section 1028.116 - General requirements for informed consent
- Section 1028.117 - Documentation of informed consent
- Section 1028.118 - Applications and proposals lacking definite plans for involvement of human subjects
- Section 1028.119 - Research undertaken without the intention of involving human subjects
- Section 1028.120 - Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency
- Section 1028.121 - Reserved
- Section 1028.122 - Use of Federal funds
- Section 1028.123 - Early termination of research support: Evaluation of applications and proposals
- Section 1028.124 - Conditions