Mr. Lieberman has over 35 years experience in medical device and pharmaceutical regulatory affairs. He was formerly a Vice President of Quality Assurance and Regulatory Affairs in industry, and prior to that with the U.S. Food and Drug Administration (FDA) where he held various positions in the Office of Compliance of the Center for Devices and Radiological Health. He also served FDA as a field investigator, performing international and domestic inspections of pharmaceutical and medical device manufacturers.
With a BS degree in Mechanical Engineering from Polytechnic University, Brooklyn, New York, and a Juris Doctor degree from Northern Kentucky State University, he is a Regulatory Affairs Certified Emeritus with the Regulatory Affairs Professional Society (RAPS), and a member of the Bar in the State of Ohio and the District of Columbia.
Mr Lieberman acts as the US Agent for Donawa Lifescience Consulting clients, providing a US-based means for the FDA to be able to make contact with non-US manufacturers. In addition, he conducts medical device quality system audits, pharmaceutical GMP audits, and pharmaceutical dietary supplement GMP audits, in the US, Europe and worldwide.