Michael Trieb is currently the Senior Director of Regulatory Affairs at Formycon AG, bringing over 20 years of international experience in regulatory affairs for biopharmaceuticals, vaccines, and biosimilars. They have extensive hands-on experience in compiling CMC documentation and leading the preparation of regulatory submissions, including interactions with various health authorities such as the FDA and EMA. Michael has previously served in senior roles at bioeq GmbH and Novartis Vaccines and Diagnostics, and holds an International Executive MBA from the Euro*MBA Consortium along with a Doctorate in Chemistry from Leopold-Franzens Universität Innsbruck.
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