Steve Strong joined Minnetronix in 2003 and has more than 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 and validation activities for medical device development and manufacturing.
Steve 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 a presenter on topics including CE marking of medical devices, corrective action/preventive action (CAPA), and the 510(k) and PMA processes.
In 2008, Steve was named Vice President of Quality and Regulatory Affairs after serving for five years as Director of Quality Assurance and Regulatory Affairs. He graduated from the University of Minnesota with a Bachelor of Science in Electrical Engineering and also holds Master in Business Administration from the University of St. Thomas.
Email Steve at firstname.lastname@example.org