Clinical Research Pre-Review Approval Process
All cancer studies involving human subjects must pass through a Cancer Clinical Research Pre-Review Approval Process before they can begin. This process is separate from the IRB approval process, but it may take place at the same time.
Get ApprovalClinical Research Program
Patients of the Cancer Institute have access to cutting-edge prevention strategies and cancer therapeutics through its clinical research program.
Clinical Trials Office
The Clinical Trials Office assists investigators with clinical trial design, regulatory management and data management.
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Disease Oriented Committees (DOCs)
The Disease Oriented Committees (DOCs) help cancer researchers identify clinical collaborators, work out feasibility issues, and brainstorm experimental and statistical design.
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Protocol Review and Monitoring Committee
The Protocol Review and Monitoring Committee provides scientific review of all clinical research at the Cancer Institute and monitors human subject accrual to clinical trials.
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Clinical Trials at the Cancer Institute
Clinical trials are research studies in which people help doctors find better ways to prevent, diagnose or treat medical conditions, including cancer.
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