Ingrid Stroo is a biopharmaceutical scientist with a PhD from the University of Amsterdam. Ingrid has held various roles in regulatory affairs, currently serving as the Director of Global Regulatory Affairs CMC at Pharming Group N.V. Ingrid's work emphasizes the development and production of biologics and plasma-derived medicinal products, and Ingrid has contributed to clinical trials and marketing applications. Previously, Ingrid conducted significant research in renal injuries and the production of coagulation factors, resulting in multiple peer-reviewed publications.
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