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Didier Relin is a seasoned professional serving as the Vice-President and Head of International Regulatory Affairs for Takeda, focusing on the EUCAN and Emerging Markets. With a Pharm D degree and a Master's in Regulatory Affairs, Didier has developed extensive expertise in US, European, and International regulations throughout a career spanning over two decades. Prior roles included leadership positions at notable organizations such as Roche, Vifor Pharma, and GSK, where Didier contributed significantly to drug registration and development across various therapeutic fields, including oncology and infectious diseases. Strong communication and leadership skills have been recognized, facilitating effective collaboration with a variety of stakeholders.