Anna Perbro is a Regulatory Affairs Manager at Galderma Nordic AB, with extensive experience in regulatory affairs spanning over a decade. Previously, Anna worked as a Regulatory Affairs Manager at Kenvue and Medivir AB, where they managed regulatory strategies and lifecycle activities for various medical products in the Nordic region. They also held roles at AstraZeneca as a Quality Assurance Officer and at Bristol-Myers Squibb as a Regulatory Affairs Assistant. Anna earned a Master of Science in Biology from Södertörn University and Stockholm University.
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