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Riki Ellison, one of the top Missile Defense Experts in the World, is Founder and Chairman of MDAA. He received his degree from the University of Southern California, including a Certificate in Defense and Strategic Studies. Mr. Ellison has more than twenty five years of experience as an advocate for the Deployment and Development of a Missile Defense System for missiles of all ranges. He has become an expert on the issue and is the Premier Spokesperson on the Nation’s Missile Defense Program.
Mr. Ellison was hired by the United Missile Defense Company in 1997, and was responsible for marketing and the business development for the lead systems integrator of the National Missile Defense System which was a requirement of the Ballistic Missile Defense Organization.
During the aftermath of the terrorist attacks on 9/11, in 2001, Ellison founded and developed the business strategy that would later become Missile Defense Advocacy Alliance in conjunction with the United States withdrawal from the anti-ballistic missile treaty and the decision by the President of the United States to deploy missile defense systems.
Mr. Ellison is a former NFL Football Player and three-time Super Bowl Champion who is a seasoned Public Speaker on the topics of Missile Defense, Defense, Football and Motivation.
John Lawrence Stevens, RAC, has over 20 years of FDA Regulatory Compliance experience encompassing virtually all FDA field positions. He also has 18 years of industry experience as a mid-level manager and senior executive in clinical, regulatory, and quality in the Medical Device Industry, including several large and small cardiovascular companies.
Mr. Stevens 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 which reviewed over 30 PMA clinical studies for cardiovascular devices. He regularly perform webinars regarding FDA and issues regarding Clinical Studies and Medical Devices.
Litigation Support - An FDA expert and seasoned business professional, Mr. Stevens is uniquely qualified to opine on cases involving the FDA's regulation of medical devices. He has served as an expert witness for over 10 court cases involving the FDA regulation of medical device firms. His services include thorough reporting, depositions, and trial testimony.
Areas of Expertise: