Eric Distad

Biography

He have over 23 years of experience in all facets of clinical research including 21 years in medical device clinical research. He joined INC Research with experience at one of the top-three medical devices companies as well as having experience in the start-up atmosphere. He have been responsible for the development and management of over forty (40) IDE studies including protocol development through final report/submission to regulatory authorities. My experience includes primarily Class III devices with indications in neurology (spinal cord and deep brain stimulation), cardiac (pacemaker, ICD, valves, LVAD, heart failure), vascular (stents), and orthopedics. Geographically, He have significant experience managing trials in the United States, Canada, Europe, and Hong Kong/China including extended assignments within these regions. He have peer reviewed publications, sat on committees establishing clinical trial standards for migraine, obesity, and Parkinson’s trials, and named on a patent for atrial fibrillation and heart failure. Through various roles within the industry,He have proven excellence in the management of clinical trials and associated regulatory interaction; therapeutic and technological expertise; and KOL development and management.

Research Interest

Medical Devices