Aditya Chauhan is an accomplished professional in the field of Global Regulatory Affairs, currently serving as Associate Director at Lotus Pharmaceutical Co., Ltd since July 2019. In this role, Aditya leads regulatory strategy and submissions for solid oral dosage forms, providing comprehensive CMC regulatory support across various regions including the US, EU, Canada, Japan, Latin America, MENA, and ASEAN. Prior experience includes a Deputy Manager position at Pfizer where Aditya focused on electronic submission requirements, and a Manager role at Sun Pharma, emphasizing submission structure strategies in compliance with regulatory guidelines. Earlier career stages include roles at Cipla and AKUMS Drugs & Pharmaceuticals, where Aditya gained extensive knowledge in regulatory compliance and submission processes. Aditya holds a Master’s degree in Pharmacy from Al-Ameen College of Pharmacy and a Bachelor’s degree in Pharmacy from U.P. Technical University.
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