Katrine holds a Master of Science in human biology and a PhD in molecular genetics. From cradle to grave of a medical device; Katrine has done it all during her 10+ years of regulatory experience in the medical device industry. Katrine loves nerding out regulations to find the smoothest and most valuable pathways to market safe and effective products. Most recently, Katrine has worked as Head of Regulatory Affairs Operation in Ambu A/S where she was responsible for developing and implementing regulatory strategies, corporate procedures and have been instrumental in successful MDR transition. An opportunity to learn a new skill? Then Katrine is at her marks and has in addition to above had her hands in vigilance, recalls, post market surveillance, design control, risk management, UDI & distributor/importer requirements. In her spare time, Katrine enjoys spending time with family and friends over a nice dinner – to compensate she does outdoor functional training all year round (yes, also when is snows!)