Resources for Clinical Researchers and GCRC Staff

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	Data Safety Monitoring Plan (DSMP) and other Clinical Trial Resources

UF GCRC Forms (some adapted from University of California San Francisco Clinical Research Office [UCSF] Documents) Protocol Feasibility Checklist (MS Word, 40kb) Clinical Trial Regulatory File Checklist (MS Excel, 20kb) Site FDA Audit Checklist (MS Excel, 22kb) Drug Accountability Form (MS Word, 58kb) Protocol Deviation Form (MS Word, 22kb)

Useful Links Websites for Regulatory Affairs National GCRC Research Subject Advocate (RSA) Web Site

Financial Conflict of Interest Association of American Medical Colleges (AAMC) (PDF File) DHHS Draft Interim Guidance

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This page is created and maintained by the DSL Manager at the GCRC of UF