Regulatory Affairs

Katja Schüz

Global Regulatory Affairs

Katja Schüz has more than 20 years of experience in the Pharmaceutical industry. She has worked with focus on Regulatory Affairs in the International / Emerging Markets and successfully contributed to various global Regulatory affairs projects and filings worldwide. Before returning to Merck KGaA, Darmstadt, Germany in June 2013 as director in Global Regulatory Affairs, she was heading Regulatory Affairs Product Strategy and CMC in H. Lundbeck A/S.

Sophie Breitenfeld

Regulatory Affairs Manager – Global Health

Sophie is a pharmacist by training and completed her postgraduate studies as a "Master of Drug Regulatory Affairs" at the University of Bonn in 2011. She joined Merck in 2008 as Regulatory Affairs Manager with a focus on Regulatory Affairs in the International / Emerging Markets. Since 2017 Sophie is involved in Merck´s Praziquantel Global Health projects and recently joined the Pediatric Praziquantel Consortium to support the registration of the pediatric formulation.