Debiopharm
Thanh Liem Vu serves as the QA Director and Qualified Person at Debiopharm Research & Manufacturing SA since March 2008, contributing as a key member of the Executive Board and overseeing compliance with over 30 regulatory authority inspections. Previously, Thanh held roles at Vifor Pharma and UCB, managing quality assurance, manufacturing processes, and validation in pharmaceutical production. Educational qualifications include a Ph.D. in Pharmaceutical Sciences and related degrees from the University of Lausanne, positioning Thanh as an expert in quality assurance and risk management within the pharmaceutical industry.
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Debiopharm
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Debiopharm Group is a biopharmaceutical development specialist that in-licenses promising biologics and small molecule drug candidates. They develop their products for global registration and maximum commercial potential for out-licensing to pharmaceutical partners for sales and marketing.