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Title 16--Commercial Practices
CHAPTER II--CONSUMER PRODUCT SAFETY COMMISSION
PART 1028--PROTECTION OF HUMAN SUBJECTS
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 | 1028.101 | To what does this policy apply? |
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| 1028.102 | Definitions. |
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| 1028.103 | Assuring compliance with this policy--research conducted or supported by any Federal Department or Agency. |
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| 1028.107 | IRB membership. |
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| 1028.108 | IRB functions and operations. |
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| 1028.109 | IRB review of research. |
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| 1028.110 | Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research. |
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| 1028.111 | Criteria for IRB approval of research. |
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| 1028.112 | Review by institution. |
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| 1028.113 | Suspension or termination of IRB approval of research. |
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| 1028.114 | Cooperative research. |
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| 1028.115 | IRB records. |
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| 1028.116 | General requirements for informed consent. |
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| 1028.117 | Documentation of informed consent. |
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| 1028.118 | Applications and proposals lacking definite plans for involvement of human subjects. |
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| 1028.119 | Research undertaken without the intention of involving human subjects. |
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| 1028.120 | Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal Department or Agency. |
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| 1028.122 | Use of Federal funds. |
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| 1028.123 | Early termination of research support: Evaluation of applications and proposals. |
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| 1028.124 | Conditions. |
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