Jette Vestergaard Olsen

Sr. Regulatory Affairs Specialist

Jette has more than 25 years of experience working with global regulatory affairs in the pharma industry. During that time, she has interacted with authorities from many different countries, including US, EU, Japan, China and Canada. Jette has been involved in several global submissions of new active substances, both as an overall regulatory lead as well as with special focus on the clinical part of the dossier and development of labelling (e.g. USPI).

Jette has led authority meetings in both Europe and US, such as national SA, EMA SA and preIND, EoP2 and pre-NDA meetings in the US.