Mireille Muller is a strategic regulatory affairs expert with a Ph.D. in organic chemistry and over 25 years of experience in the pharmaceutical industry, including two decades at Novartis. Currently, Mireille works as an independent consultant in regulatory affairs, assisting healthcare companies with regulatory processes and focusing on development. Previously, Mireille held various roles in regulatory affairs, including leadership positions in drug development and policy at Novartis and other organizations. Fluent in French, German, and English, Mireille collaborates with Swiss and European clients to navigate complex regulatory environments.
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