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Sudeepthi B is an experienced regulatory affairs and drug safety professional with a diverse background in the medical device and pharmaceutical industries. Sudeepthi held the positions of Senior Regulatory Affairs Specialist, IVD Medical Device Regulatory Affairs Specialist III, and IVD Medical Device Regulatory Affairs Specialist II at Cepheid. Prior to that, Sudeepthi worked as a Drug Safety Specialist at IQVIA and United Biosource Corporation and gained early experience as a Quality Control Analyst at Cipla and a Hub Labeling Manager at Pfizer. Sudeepthi holds a Doctor of Pharmacy (Pharm.D) from Manipal Academy of Higher Education and an MBA in Health Care Services from Sikkim Manipal Institute of Technology.