J.Lawrence Stevens
J.Lawrence Stevens
Mr. J Lawrence Stevens has over 20 years of FDA experience encompassing virtually all of the FDA field positions. Also Mr. Larry has eighteen years of industry experience as a mid-level manager and senior executive in clinical, regulatory, and quality in the medical device industry. Mr. J Lawrence 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 to audiences ranging from senior executives, physicians, technical personnel, other medical personnel, major media, and the general public.
Live Webinar
Recorded Session
FDA's Enforcement Strategy for Mobile Medical Applications
The marriage of mobile applications to medical devices is the latest and will be a future trend in medical devices. The scenario could be developing an APP to allow access to your device. &n…
Industry: FDA Compliance Duration: 60 Minutes