Arvind Mathuria is currently the Associate Director of Regulatory Affairs at Cipla, where they lead a team responsible for the filing of Abbreviated New Drug Applications (ANDAs), deficiency responses, and post-approval changes. With 17 years of experience in Regulatory Affairs for the US market, Arvind has comprehensive expertise in managing submissions from strategy and planning through to post-approval maintenance. Prior to Cipla, they worked as a Research Associate at Ranbaxy, focusing on the development and validation of HPLC methods and handling deficiency responses related to analytical processes. Arvind holds an M. Pharm. degree in Medicinal Chemistry from the Bombay College of Pharmacy.
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