Yingying Liu is a seasoned regulatory professional with experience in manufacturing operations, quality assurance and regulatory affairs in China, Europe and USA. She holds an M.Sc. in pharmaceutical science and an M.Sc. in regulatory affairs and health policy.
She has managed many high-quality Clinical Trial Applications, Marketing Authorisation Applications and post-approval change applications in China and in Europe. She advices companies on the best possible application pathways, particularly for biological drugs. Her particular expertise is in the field of biological licence applications in China.
She regularly publishes articles and book chapters, and delivers lecturers and training in new regulatory developments and submission management.
Wednesday, October 28, 2020
08:30 – 09:00 CET
Friday, October 30, 2020
09:15 – 09:45 CET