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Seppe De Gelas is the VP of Regulatory Affairs and Quality Assurance at Hyloris Pharmaceuticals, where they oversee international regulatory affairs and quality assurance in pharmaceutical development and manufacturing. Seppe has accumulated over 20 years of experience in the industry, having held key roles at organizations including Baxter Hemoglobin Therapeutics, UCB Pharma, GSK, and Lonza Braine SA. Additionally, Seppe serves as a lecturer on European Regulatory Affairs at the University of Georgia's College of Education, focusing on preparing students for careers in regulatory affairs. Seppe obtained a master's degree from VUB in 1993.