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Margrethe Erbou Andersen has extensive experience in regulatory affairs, with a focus on clinical development pipeline activities. Margrethe has held various leadership roles in regulatory affairs at companies such as Galecto, Inc., IWA Consulting, and H. Lundbeck A/S. Margrethe has also worked as a Guest Lecturer at Atrium Copenhagen and started their career as a Regulatory Affairs Specialist at Hexal A/S. With a MSc (Pharm) degree from the University of Copenhagen, Margrethe's expertise lies in regulatory documentation preparation, submissions, and regulatory agency interactions.