Larissa Milke

Larissa Milke, PhD, is an accomplished professional in the field of regulatory affairs, currently serving as the Director of Global Regulatory Affairs CMC at CSL since August 2013, with a focus on gene therapy and advanced therapy medicinal products (ATMPs). Prior roles at CSL include Associate Director and CMC Regulatory Lead, demonstrating extensive expertise in regulatory strategy for complex biotechnology products. Before joining CSL, Larissa Milke worked as a Research Associate at the Institute of Pathobiochemistry at University Hospital Frankfurt am Main from May 2008 to January 2013. Larissa Milke holds a PhD in Biochemistry from Goethe University Frankfurt and a Diplom in Biology from RWTH Aachen University.