Gitte Tange

VP, Regulatory Affairs and Clinical Development, Senior Regulatory Affairs

Gitte has more than 20 years of experience with regulatory affairs within both life cycle management and drug development. She is a very skilled project manager, who is excellent in communicate with and engage stake holders. Gitte has worked on a diverse range of regulatory submissions, among others CTA, IND, Orphan Drug Designations, Agency meetings (National, EMA and FDA) and MRP/DCP.