Our site utilizes Central IRB's to facilitate rapid study start up. Our department can expedite regulatory submission of all essential regulatory documents, such as 1572, financial disclosure, IRB submission forms, and consent forms within 2-3 business days. Our site has SOP's in place. All investigators and staff have been trained in GCP and ICH guidelines. MD Clinical follows strict HIPPA and PHI policies to protect our study patients' privacy. More information is available upon request.