| Research Compliance / | ||||
| Belmont Report | ||||
| Ethical Principles and Guidelines for the Protection of Human Subjects of Research, The National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, April 18, 1979 | ||||
| Confidentiality Certificates |
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| Declaration of Helsinki |
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| FDA | ||||
| * | Information Sheets for IRBs, Clinical Investigators and Sponsors | |||
| * | Good Clinical Practice in Clinical Trials |
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| OHRP | ||||
| * | Policy guidance by topic | |||
| * | Links, maintained by OHRP, to other human subject protection sites including historical and international documents | |||
| * | Frequently asked questions | |||
| * | Summary of compliance determinations | |||
| Self assessment tool for IRBs | ||||
| Office of Research Integrity (ORI) | ||||
| Regulations | ||||
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| * | DHHS: 45 CFR 46 Protection of Human Subjects | |||
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| * | FDA: 21 CFR 50 Protection of Human Subjects | |||
| * | FDA: 21 CFR 56 | |||
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