Mr.Larry Stevens

Mr. Larry Stevens has over 20 years of FDA experience encompassing virtually all of the FDA field positions. He also has eighteen years of industry experience as a mid-level manager and senior executive in clinical, regulatory and quality in the medical device industry. He has personally designed quality systems, prepared regulatory submissions (510(k), IDE and PMA) and managed 7 multi-center clinical trials for class 3 medical devices. From 1989-1993, he was the Industry Representative on the FDA Circulatory Systems panel. Finally, he is a seasoned educator/speaker with over 250 public presentations and 20 webinars to audiences ranging from senior executives, physicians, technical personnel, other medical personnel, major media and the general public. He also serves as an Expert Witness in cases involving medical devices and FDA regulations.