I have experiences from positions at the Norwegian Medicines Agency (NoMA), LINK Medical Research and Weifa. At NoMA I worked with assessing Variation- and MA applications for human vaccines. At LINK Medical Research I worked for several different pharmaceutical companies, mainly with regulatory affairs for human medicinal products, but also with other product classes. At the R&D department at Weifa I ensured post-approval maintenance of existing MAs. I also outlined regulatory strategies for applications for new MAs, and managed the applications through to approval.

Via my Regulatory consultancy company, I have gained experience with products for farmed fish (medicines, feed additives, biocides), including regulations applicable for R&D projects. I have also gained experience with writing and compiling CMC documents for Variations.

My background is MSc and PhD in biochemistry and toxicology from the University of Oslo. The doctoral work was performed at Oslo University Hospital, where I also had a post-doctor position. I started my education with BSc in Environmental sciences at Telemark University College.