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Informed Consent
Institutional Review Board (IRB)
Adverse Event/Protocol Deviation
Clinical Research Policy Manual
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IRB Application
(.docx, 649K)
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IRB Application
Research Team Attachment
(.docx, 652K)
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Research Team Attachment
Subjects PHI Authorization Form
(.docx, 641K)
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Subjects PHI Authorization Form
Appendix A - Research Equipment Form
(.docx, 644K)
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Appendix A - Research Equipment Form
Appendix B1 - Device Form
(.docx, 665K)
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Appendix B1 - Device Form
Appendix B2 - Drug and Chemical Usage Form
(.docx, 664K)
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Appendix B2 - Drug and Chemical Usage Form
Local Contextual Review
(.docx, 641K)
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Local Contextual Review
New Protocol Application Form
(.docx, 695K)
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New Protocol Application Form
Human Research Protection Education Training PI Investigator
(.docx, 639K)
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Human Research Protection Education Training PI Investigator
PI responsibility form
(.docx, 647K)
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PI responsibility form
Required Product Information
(.docx, 646K)
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Required Product Information
Appendix C - Biological Materials Form
(.docx, 646K)
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Appendix C - Biological Materials Form
IRB termination form
(.docx, 631K)
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IRB termination form
Research Insurance Coverage protocol
(.doc, 600K)
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Research Insurance Coverage protocol