Who we are

The highly qualified personnel who operate EPIC will act as resources to assist clinicians and researchers in developing robust translational data to support the clinical development of their products. The EPIC team will provide scientific input on trial design, regulatory oversight and assist in product development issues related to manufacturing for clinical trial applications, release criteria, potency and sterility testing. In addition the team will be available for consultation in the strategic planning and writing of protocols for submission to the IRB and FDA.