Dr Rose Quadbeck-Diel

Head of Regulatory Affairs

Dr. Quadbeck-Diel joined us in 2006 as Senior Manager Regulatory Affairs before taking over responsibility as Head of Regulatory Affairs in 2009. She is responsible for planning and submission of marketing authorisation applications as well as life cycle management of centrally authorised products in the EU. Prior to joining us, Dr. Quadbeck-Diel served as Head of Regulatory Affairs in international companies where she was responsible for performing national and MRP application procedures. Dr. Quadbeck-Diel holds a PhD from the Clinical Centre of the University of Frankfurt/Germany.