Peter Carlyle

Mr. Carlyle joined CardioMed Device Consultants in January 2017. Peter has over thirty years’ experience in directing all aspects of clinical and regulatory affairs in both academic and industrial settings. He possesses a deep and broad expertise in cardiovascular, vascular and orthopedic (spine) devices including cerebral, carotid, coronary, and peripheral artery stents and balloons, AAA grafts, percutaneously delivered heart valves, mitral valve repair devices, and injectable products for degenerative disc disease. Mr. Carlyle’s relationship with cardiovascular medicine began at the University of Minnesota directing the core heart failure research laboratories, both in basic science and clinical research. This was followed by a long career in industry involving executive and leadership positions in Clinical Affairs departments for large, medium, and small device manufacturers. Work groups environments ranged from a single employee (myself) to 40 employees world-wide. Additionally, he has extensive experience in the design and operation of European device trials and FDA audits of offshore investigational studies. Currently, for CardioMed, Peter provides clinical studies project management for offshore companies in preparation for global IDE studies