Rich has a broad background in medical device company operations coupled with ISO and FDA regulatory experience. He has successfully navigated FDA and ISO audits and has played a pivotal role in submitting medical devices for 510(k) approval as well as maintaining ISO 13485 quality management systems for medical devices. His operations, manufacturing, and project management background provide a wealth of knowledge that will improve the success of all projects. His extensive network of medical device manufacturers ensures that your product will take advantage of the newest advancements in medical device manufacturing. Rich studied Electrical Engineering at the University of California at Davis.
Current role