Cepheid
Scott Campbell is an accomplished professional in regulatory and clinical affairs with over 20 years of experience in the molecular diagnostics industry. Currently serving as Senior Vice President of Regulatory and Clinical Affairs at Cepheid since June 2010, Scott manages global teams to deliver product validations and registrations. Previous roles include Senior Vice President and General Manager of Oncology and Corporate Vice President and Chief Regulatory Officer at Cepheid, where responsibilities encompassed P&L management, strategic planning, and clinical trial execution. With a progressive career spanning several companies, including Nanosphere and Third Wave Technologies, Scott has expertise in clinical trial design, commercialization of diagnostic products, marketing, and product development. Scott holds a PhD in Cell, Molecular, and Developmental Biology, an MBA in Management, and degrees in Botany and Biology from the University of Wyoming and the University of California, Riverside.
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Cepheid
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Cepheid is a molecular diagnostics company. The Company develops, manufactures and markets fully-integrated systems for testing in the Clinical and Non-Clinical markets. The Company's systems enable molecular testing for organisms and genetic-based diseases by automating otherwise complex manual laboratory procedures. The Company's systems integrate these steps and analyze biological samples in test cartridges. Its primary offering is the GeneXpert system, which integrates sample preparation in addition to Deoxyribonucleic acid (DNA) amplification and detection. The GeneXpert system is designed for a range of user types ranging from reference laboratories and hospital central laboratories to satellite testing locations, such as emergency departments and intensive care units within hospitals, as well as physician offices and other alternate site laboratories. It also offers the SmartCycler system, which integrates DNA amplification and detection to allow rapid analysis of a sample.