Chueng Kee

Senior Director, Regulatory Affairs at Lonza

Speaker

Kee Cheung leads Regulatory Affairs for Integrated Biologics at Lonza. She has been in the Biopharmaceutical industry for over twenty years with vast experience leading regulatory organizations to support Customers across multiple technologies (mammalian, antibody drug conjugates and drug product manufacturing). Kee specializes in Regulatory CMC is responsible for global license and clinical applications including the US FDA, EMA and in China. Earlier in her career, Kee held Quality and Analytical roles. She holds a B.Sc. (Hons) in Biochemistry from Kingston University, UK