Lawerence Stevens Mr. Stevens has a unique background of FDA and Industry experience. He 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, was the Industry Representative on the FDA Circulatory Systems panel which reviewed over 30 PMA clinical studies for cardiovascular devices. He currently serves as an expert witness for cases involving FDA regulation compliance for medical devices. He regularly performs webinars regarding FDA and issues regarding clinical studies and medical devices. Finally, he is a seasoned educator/speaker with over 150 public presentations to audiences ranging from senior executives, physicians, technical personnel, other medical personnel, major media, and the general public.
If you work for any firm that manufactures products regulated by FDA, you very likely will experience an FDA inspection.
Speaker: Larry Stevens | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View DetailsDuring this webinar we will provide information on the backgrounds of FDA employees, how FDA employees are trained, how they interact with the regulated industry.
Speaker: Larry Stevens | View Anytime | Duration: 60 Minutes | Price: ¤199.00 | View DetailsIf you work for any firm that manufactures products regulated by FDA, you very likely will experience an FDA inspection.
Speaker: Larry Stevens | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View DetailsDuring this webinar we will provide information on the backgrounds of FDA employees, how FDA employees are trained, how they interact with the regulated industry.
Speaker: Larry Stevens | View Anytime | Duration: 60 Minutes | Price: ¤399.00 | View Details