Katrien Oosterom is a Senior Vice President of Regulatory Affairs with a wealth of experience in pharmaceutical, healthcare, and quality control roles spanning over two decades. Oosterom has held various titles such as Manager Quality Control/Qualified Person and Regulatory Affairs Scientist, where Katrien has been responsible for writing regulatory submissions and communicating with Health Authorities globally. With a background in Clinical Information Analysis and Quality Assurance, Oosterom brings a broad skill set to their current role at C² PHARMA.
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