Steve Strong has over 20 years of experience in quality assurance and regulatory affairs in the development of electronic products for the medical device industry. For the past 17 years he has managed quality systems and product verification/validation activities for the development and manufacturing of medical devices.

He has extensive experience with product safety and EMC testing and has served on various committees for international standards development and product safety standards. He is the author of numerous articles and presenter on topics including CE marking of medical devices, corrective action/preventive action (CAPA), and the 510(k) and PMA processes.

Steve serves as the VP of Quality and Regulatory Affairs after serving for five years as Director of Quality Assurance and Regulatory Affairs at Minnetronix. He graduated from the University of Minnesota with a Bachelor of Science in Electrical Engineering and also holds an MBA from the University of St. Thomas.