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Director Regulatory Affairs & Quality Assurance

Substantial career in global regulatory affairs in a broad range of therapeutic areas, ranging from infectious diseases to oncology.

Extensive experience supporting global development programs in various stages of development and leading discussions with the U.S. Food and Drug Administration (FDA) , the European Medicines Agency (EMA) and other regulators.

Worked with a multitude of biotech companies over the last decade, helping them advance the development of their products.

Serving on the advisory board of a number of companies, translating scientific and clinical strategies to a regulatory approach.

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