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Checklists provide support for investigators and the IRB when research meets certain sets of regulatory criteria. Checklists do not need to be completed or retained by investigators, but should be used as tools when drafting research protocols.
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The emergency use form and visitor confidentiality agreement are included in this folder.
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The Human Research Protection Plan and Investigator Manual are included in this folder.
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Standard Operating Procedures (SOPs) relevant to investigators, such as SOPs related to informed consent, conflicts of interest, and definitions are included in this folder.
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Protocol templates, sample protocols, and informed consent templates can be found in this folder. USF investigators are required to use a USF IRB protocol template included in this folder.
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Worksheets provide support for investigators and the IRB when research meets certain sets of regulatory criteria. Worksheets do not need to be completed or retained by investigators, but should be used as tools when drafting research protocols.
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