This application will be submitted to the CRC Advisory Committee, which meets on a monthly basis to review new study protocols in the CRC. A complete application will include this form & attachments (study schematic, IRB protocol, and Informed Consent form), and a Data & Safety Monitoring Plan (usually part of the IRB application).

All studies carried out in the CRC must be approved by the IRB and the CRC Advisory Committee. Submission to both may be made concurrently.

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