Christopher DiMatteo has over 20 years of experience in the medical device industry. Christopher's professional journey encompasses the successful management of clinical trials across a range of perspectives, including hospitals, contract research organizations (CROs), and major medical device manufacturers. Throughout his career, he has navigated numerous clinical trials with diverse objectives, such as securing PMA approvals, fulfilling FDA-mandated post-approval requirements, conducting investigator-initiated studies, and spearheading pivotal marketing investigations. His expertise extends to the design and implementation of studies that comply with both domestic and international regulations, guiding medical devices from their conception to regulatory approval.