Cepheid
Sharmin Bhathena, MS, RAC (US, Global) currently serves as the Senior Manager of Regulatory Affairs at Cepheid since September 2020. Prior experience includes managerial roles in regulatory affairs at Roche, focusing on genomics and oncology companion diagnostics, and at Abbott, which is now part of Johnson & Johnson Vision. Sharmin's career also encompasses positions as a Regulatory Affairs Specialist at Thermo Fisher Scientific and Optovue, and as a Regulatory Affairs/Quality Assurance professional at Keck Medicine of USC. Early career experience includes a regulatory affairs internship at Life San CRO. Sharmin holds a Master's degree in Biomedical Engineering from the University of Southern California and a Bachelor's degree in Instrumentation from the University of Mumbai.
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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.