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Rose Griffith - Director of Clinical Affairs. Ms. Griffith's 29-year professional career has included 18 years of direct patient care and over 11 years of experience in the medical device industry. Her clinical responsibilities included procedural assistance to physicians and chart management as well as local site coordination of research studies and educational activities. In the medical device industry her efforts have included both implantable devices and diagnostic capital equipment. Ms. Griffith has been responsible for monitoring operations and managing multiple clinical trials necessary for regulatory approval through IDE/PMA (Class III devices) and post-market adoption of 510(k) products. She has co-authored numerous science studies that have been presented and published in the medical literature. | 