Nitish Parekh is a regulatory affairs professional specializing in medical devices and combination products, with over 10 years of experience in the pharmaceutical industry. They have held positions at Pfizer, including Principal Medical Device Engineer and Manager of Regulatory CMC Strategy, and have also worked as a Regulatory Affairs Officer at Roselabs Bioscience Ltd. Nitish served as a Project Trainee in formulation development at CADILA HEALTHCARE LTD. Currently, they are the Associate Director of CMC Regulatory Affairs for MDCP at AstraZeneca. Nitish holds a Bachelor of Pharmacy from Gujarat University and a Master of Pharmacy in Pharmaceutics and Drug Design from Gujarat Technological University, Ahmedabad.
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