Born 1966. VP of Regulatory Affairs & QA. Joined in 2020.
Professional background: Marie Källström has more than 25 years global experience from Regulatory Affairs positions in late-stage pharmaceutical development in companies such as Pfizer, AstraZeneca and Pharmacia. The last position was Regulatory Specialist at Novo Nordisk with responsibility for coordinating the development of NDA/MAA documentation as well as planning and participation several Authority interactions within the development of pharmaceutical products for treatment of diabetes and obesity. Marie joined Ascelia Pharma as Director of Regulatory Affairs. She got her current role and became a member of the Management Team in 2022.
Education: M.Sc. in Biology at Lund University, Sweden
Other ongoing assignments: None
Holdings in Ascelia: View holdings