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A special advisor to Tunnell Consulting in the areas of regulatory strategy, R&D, and clinical manufacturing, Alex is a respected U.S. and foreign regulatory expert who brings exceptional industry knowledge to our firm. He is a former Senior Vice President of Worldwide Regulatory Affairs at Schering-Plough Research Institute, a former Senior Vice President of Global Compliance at Schering-Plough Corporation, and was one of the original members of the steering committee of the International Conference on Harmonization, where he introduced the concept of the common technical document (CTD). His extensive pharmaceutical industry career also includes numerous professional and academic positions, including serving as chairman of the Regulatory Affairs Coordinating Committee of the Pharmaceutical Research and Manufacturers Association, lecturing on drug law at Temple University, and serving on the planning committee at the University of Texas for their program on the International Conference for Drug Development. Alex is a member of numerous professional associations and uses his more than 30 years of expertise to help foster advancement in the life sciences environment at a time of critical and widespread industry change.
Dr. Giaquinto received a Ph.D. in Pharmaceutics from University of Connecticut and a B.S. in Pharmacy from St. John’s University College of Pharmacy. | 