Bart Baert is a regulatory affairs professional with approximately 20 years of experience, specializing in chemical drugs. They began their career as a QA Compliance Officer at Alcon Laboratories, where they developed skills in writing CMC sections. At Baxter Healthcare, Bart advanced through various roles, eventually becoming a leader in European Regulatory Affairs, mastering regulatory procedures and licensing activities. Currently, Bart serves as the Director of Global Regulatory Affairs, CMC at UCB, focusing on small molecules and drug-device combination products, while previously pursuing NDA approvals in Japan and China. Bart holds a Master of Science in Pharmaceutical Sciences and a Specialization in Industrial Pharmacy from Universiteit Gent.
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