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Dr. Maderazo serves as the Vice President, Quality, Regulatory, and Clinical Affairs and has held various roles with the company since joining in September 2013. Dr. Maderazo has over 19 years of quality, regulatory, and clinical experience in the medical device industry where he has championed organizational quality compliance and has established successful regulatory strategies for numerous novel molecular diagnostic products. Prior to GenMark, Dr. Maderazo held roles of increasing responsibility in Regulatory Affairs for Hologic and Abbott Vascular. Dr. Maderazo received his B.S in Molecular & Cellular Biology from the University of Connecticut and his Ph.D. in Molecular Genetics & Microbiology from the University of Massachusetts Medical Center.