Subhash Dhende has extensive experience in regulatory affairs within the pharmaceutical industry, beginning with a trainee position at Glenmark Pharmaceuticals from December 2015 to June 2016, where responsibilities included CTD dossier preparation and filing for product registrations and renewals. Since July 2016, Subhash has been working as a Regulatory Affairs Associate at Cipla, managing product life cycle activities, assessing change controls, and compiling post-approval submissions for various markets. Prior experience includes a student internship at Dr. Bhanuben Nanavati College of Pharmacy, focusing on stability indicating assay method development and validation. Subhash holds a Master’s Degree in M.pharm QA from the University of Mumbai and a Bachelor’s Degree in Pharmacy from the University of Pune, graduating with First Class honors.
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