MRU works with both local and central IRB’s. Confidentiality agreements are reviewed, signed and forwarded to the CRO or Sponsor within 1 busines day. Upon receipt of a protocol, the MRU staff and physicians will review the study documents within 3 days. All regulatory documents will be completed and submitted within 5 business days. MRU utilizes the “Clinasyst” software data package for the management of clinical trial data, subject visits and administrative functions. This allows rapid and easy access to study data. All subject visits information is entered into case report forms (CRF’s) within 24 hours of the subject visit.

All contracts and budgets are reviewed and executed internally by the MRU administrative staff and directors. Budget reviews takes 2 days. MRU is very aware of the tremendous costs of performing clinical trials today, and we work very diligently to perform studies within the budget allocated.