Maria Risberg is a Senior Regulatory Affairs Consultant with over 20 years of experience in global drug regulatory strategy and submissions. They presently offer freelance services through MARA Consulting, focusing on regulatory strategy and project leadership for pharmaceutical, biotech, and medtech companies. Previously, they served as an Associate Regulatory Project Director at AstraZeneca, where they led global regulatory submission teams across multiple markets. Maria holds a Master of Science in Pharmaceutical Bioscience from Göteborgs universitet, obtained in 2003.
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