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Lina Påve is a regulatory CMC specialist. After many years as a quality assessor at the Swedish Medical Products Agency, she has solid experience in assessing module 3 documentation for a wide range of pharmaceutical substances and formulation forms. With her skills she becomes an important part of the team when we help our customers with gap analyses, scientific advice, and applications for marketing authorisation.
”I am really excited to be part of RegFile, a new company with a lot of commitment – and at the same time has such an experienced and knowledgeable team. The fact that we have offices in the beautiful Eklundshof next to the Uppsala Science Park and the Medical Products Agency is also a plus!”
