Cepheid
Praveen Chandrakar is a seasoned professional in the field of regulatory affairs, currently serving as Sr. Manager-International Regulatory Affairs at Cepheid since April 2018, where responsibilities include managing regulatory submissions and interactions with agencies in Greater India and South East Asia. Prior experience includes roles such as Assistant Manager-RA at Medtronic, overseeing regulatory compliance and submissions in the Indian Subcontinent, and RA/QA Specialist at St. Jude Medical, coordinating document availability for regulatory registrations. Praveen's career began as an Associate in Regulatory Affairs at Abbott, following a traineeship at Philips, and is underpinned by a Master's Degree in Pharmaceutical Regulatory Affairs from Manipal Academy of Higher Education and a Bachelor of Pharmacy from Guru Ghasidas University.
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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.