Renee D.

Renee D. is a lead consultant in Drug Regulatory Affairs with over a decade of experience in interpreting regulatory guidelines and coordinating submissions. Currently, they hold multiple roles at Genpact, including Lead Consultant for Submission Planning and Regional Regulatory Operations, where they also focus on training and mentoring colleagues. Renee previously worked at NEM Laboratories Private Limited and Inga Laboratories P. Ltd in regulatory affairs roles, building a strong foundation in the field. They earned a Bachelor of Pharmacy from M.E.T. Institute of Pharmacy from 2007 to 2011.