Radha Joshi

Radha Joshi is a highly skilled professional in regulatory affairs and pharmaceutical development with extensive experience in the biotechnology sector. Currently serving as a Senior Regulatory Affairs Specialist at IQVIA since February 2022, Radha previously held roles at SUN PHARMA where responsibilities included CMC quality and regulatory compliance, as well as analytical method development. Prior to that, experience as an Executive GMP Coordinator at Lupin involved managing change controls and quality management documentation. Radha also worked at Biocon focusing on intellectual property related to NBE and biosimilars, conducting patent searches and drafting applications. Educational background includes a Master of Science in Pharmacy (Biotechnology) from the National Institute of Pharmaceutical Education and Research and a Bachelor of Pharmacy from Gujarat Technological University.