Cornelia Ulm is a seasoned Regulatory Professional with extensive international experience in biosimilars and biotechnologically manufactured products. Having held key roles such as Director of Regulatory Affairs at Serono International and Mylan GmbH, and currently serving as Director of CMC Regulatory Affairs at GSK, Ulm specializes in regulatory strategy throughout the drug development lifecycle. Fluent in German, English, and French, Ulm is recognized for strong organizational skills and effective communication in multicultural environments. They have contributed to substantial regulatory advancements across multiple therapeutic areas, including oncology, dermatology, and rheumatology.
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