Dr. Sarika Pardhe has over 16 years of Pharma Industry experience with the main area of expertise is Global Drug Regulatory Affairs. She leads various positions in QA, R&D, Regulatory Affairs and Pharmacovigilance department with progressive and diversified accountabilities in various Pharma companies. Her experience and well understanding of diversified area help her to contribute to the different facets of the Generic Drug Industry. She has completed her master degree in Pharmacy in 2004. Further, she received her RAC credential from the RAPS/USA in 2013 and Ph.D. in Pharmaceutical Sciences in 2019.
Dr. Sarika Pardhe interest primarily includes the Global Drug Regulatory Affairs, Pharmacovigilance, Clinical Research, Regulatory Strategy, Regulatory analysis, and intelligence for all types of medicines including emergency and critical care medicines.