Anke Dr Baumann

Anke Dr. Baumann is a Regulatory CMC Writing Manager at Merz Therapeutics, with 15 years of global experience in Regulatory Affairs. They previously held positions as Regulatory Affairs Manager at Fresenius Kabi and Junior Manager Regulatory Affairs at STADA Group. Anke earned a doctoral degree in Biology from Johann Wolfgang Goethe-Universität Frankfurt am Main, which supports their biological background in Genetics and Microbiology. Their expertise includes creating CTD/ACTD data, preparing submissions for variations and renewals, and regulatory coordination for new projects.