Vice President Regulatory Affairs
Teva Pharmaceuticals
A business savvy senior regulatory leader with more than 18 years all-round experience in all aspects of regulatory affairs with a scientific background and a good understanding of the pharma business. Previous stints in Regulatory Compliance, Labeling, Strategy etc. In depth experience working with European health authorities(EMA/CHMP) as well as with various international markets. Proven experience of setting up and running regulatory departments in start-ups, midsize pharma as well as big pharma companies. Experience with biologics as well as small molecule drugs and medical devices with Health Authorities across the world. Experience with early development, late development as well as lifecycle management in various therapeutic areas. Thought leader, speaker and author on topics related to regulatory science. Extensive experience with development, registration and lifecycle management of Biologics and Biosimilars.
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Patient-Centric Endpoints and Use of Digital Health Technologies
Wednesday, May 8, 2024
11:45 – 12:45 CEST