Murat Karadeniz

Murat Karadeniz is an accomplished regulatory affairs professional with extensive experience in Chemistry and Nuclear Technology. Currently serving as Director of Regulatory Affairs CMC at Sarepta Therapeutics since June 2020, Murat previously held roles as Associate Director and Senior Manager in Regulatory Affairs CMC at GSK and TESARO, respectively. With a foundational background at Sanofi spanning nearly a decade, Murat excelled as Associate Principal and Senior Regulatory Affairs Associate, where responsibilities included leading global regulatory CMC strategies and submissions for commercial biological products across multiple international markets. Murat’s expertise encompasses strategic direction for regulatory compliance, complex regulatory analyses, and oversight of CMC filing requirements throughout various stages of product development.