Director
PwC
Overview
Megha is a director with PwC’s Pharmaceutical Advisory practice primarily focused on global regulatory strategy and operations, pharmacovigilance, and quality. She has more than 11 years of experience working with pharmaceutical, medical device, and digital health companies, both as a consultant and in industry delivering large-scale, multi year, strategic and implementation programs across R&D, manufacturing, and commercial.
Relevant experience
Led the development, design, and implementation of cross-functional Regulatory Information Management (RIM) strategy across multiple clients.
PwC Advisory Board member leading development of regulatory intelligence platform, which included tracking and assessing global regulations and providing insights.
Led a two-year process redesign and refinement effort for a global regulatory organization by defining future-state vision, reviewing over 150 procedures, and leading over 250 process design sessions, interlinking with technology platforms and driving change management strategy, including enhanced training delivery.
Led multiyear regulatory integration programs globally (MA transfers, branding/label changes, QPPV/locally responsible changes, etc.) for multiple clients.
Led program to draft, review, and publish regulatory submissions for over 80 countries.
Education
Megha has an MS in Biomedical Engineering with a minor in Regulatory Affairs from the University of Southern California and a BEng in Chemical Engineering from RVCE., India.
Disclosure information not submitted.
Tuesday, September 13, 2022
11:15 AM – 11:45 AM MST