Eva Bøge

Eva Bøge started their career in 2004 as a Regulatory Affairs Specialist at H. Lundbeck A/S. Eva was later promoted to Specialist, Regulatory Strategy Leader and was responsible for the global regulatory strategy for development compounds in various stages. In 2012, they worked as an RA Professional at LEO Pharma before joining Lundbeck in 2013. At Lundbeck, Eva held roles such as Senior Specialist in Regulatory Product Strategy, Global Regulatory Lead, Senior Regulatory Product Lead for the Brintellix Science Team, and Regulatory Strategy Leader. In 2017, Eva joined Zealand Pharma as a Senior Regulatory Project Manager and later became the Regulatory Project Director.

Eva Bøge obtained their Master's degree in Pharmacy from an undisclosed institution between 1999 and 2004. Eva then went on to pursue a Master's degree in Industrial Drug Development (MIND) at the University of Copenhagen, completing their studies from 2008 to 2016.