Pradnya Bhagwat
About Pradnya Bhagwat
Pradnya Bhagwat is a Senior Director of Regulatory Affairs at Travere Therapeutics, with over 17 years of experience in the pharmaceutical and biotech industries. She has held various regulatory roles at organizations such as IQVIA, Clinipace Worldwide, and Pfizer Global R&D, and has advanced academic qualifications in Pharmaceutical Science and Bioscience Regulatory Affairs.
Work at Travere Therapeutics
Pradnya Bhagwat serves as the Senior Director of Regulatory Affairs at Travere Therapeutics. She has held this position since 2021, contributing her extensive knowledge and expertise in regulatory processes within the pharmaceutical and biotech sectors. Her role involves overseeing regulatory strategies and ensuring compliance with industry standards, which is critical for the successful development and approval of therapeutic products.
Previous Experience in Regulatory Affairs
Prior to her current role, Bhagwat worked at IQVIA as Associate Director of Regulatory Affairs from 2017 to 2019. She also held the position of Director of Regulatory Affairs at IQVIA from 2019 to 2021. Her experience includes three years as Regulatory Strategic Development Manager at Clinipace Worldwide from 2014 to 2017, and two years as Regulatory Affairs Specialist at the same company from 2012 to 2014. Additionally, she worked at CBR International Corp. as a Regulatory Affairs Associate from 2010 to 2012.
Education and Expertise
Pradnya Bhagwat holds a Bachelor of Pharmacy (B. Pharm) degree from the University of Mumbai, where she studied from 1998 to 2002. She further advanced her education with a Master of Pharmacy (M. Pharm) from the same university, completing her studies from 2002 to 2004. Bhagwat also earned a Master of Science (MS) in Bioscience Regulatory Affairs from The Johns Hopkins University, studying from 2008 to 2011. Her educational background supports her professional focus on drug development and regulatory affairs.
Career Background in Pharmaceutical Industry
Bhagwat has over 17 years of experience in the pharmaceutical and biotech industries, with a strong emphasis on regulatory affairs. She began her career as an Associate Biometrician at Pfizer Global R&D in 2004. Her career trajectory includes various roles that have equipped her with a comprehensive understanding of regulatory processes, drug development, and compliance across different organizations.