Åsa Jansson to RegFile

We are strengthening the group within medical & regulatory writing. Åsa with her particular interest in writing scientific texts on complex subjects, will complement RegFiles perfectly. She has a Ph D in immunology and is experienced in drug development and in the writing of scientific overviews.  ”It feels exciting and stimulating to work with such… Fortsätt läsa Åsa Jansson to RegFile

Lina Påve to RegFile

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… Fortsätt läsa Lina Påve to RegFile