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Our medical team prides itself on providing rapid start-ups, speedy, accurate project management and efficient protocol achievement.
• We have rapid start up capabilities with our efficient submission techniques, as we can obtain approval and begin studies within several days of receiving final protocol.
• We have a precise chain of custody for vital documents and investigational substances with our innovative tracking system.
• In order to stringently comply with regulations regarding the protection of human research patients and ensure rapid expedited and unconditioned approvals, we maintain a database of FDA inspected Institutional Review Boards in addition to our central IRB.
• Our medical staff can promptly identify and track even the most complicated patient populations with our unique and innovative clinical trials management system. In an ever-evolving industry where accuracy is critical, data is sensitive and timing is vital, this state-of-the-art, efficient data management system is essential.