Tine Juul Zachariasen, Regulatory Affairs Specialist Medical Devices, Novo Nordisk A/S
Tine has more than 17 years of experience working with medical devices and the device part of drug-device combination products. For the past 10 year she has worked with several device constituent development projects for e.g., prefilled pens and has been responsible for the regulatory files for the device constituent part submitted to e.g., EMA and FDA.
Tine previously worked in the Device Department at the Danish Medicines Agency where she worked with Vigilance and Market Surveillance and acted as the Danish representative in the EU commission Working Groups for Vigilance and Market Surveillance.
Tine holds a MSc in Biology from the University of Copenhagen.