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Thursday, June 18 • 5:00pm - 6:00pm
#555 OD: ON DEMAND - Updates of Drug Evaluation and Inspection in China

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Component Type: Forum
Level: Intermediate

This forum will include discussions and updates from CCDIE and NMPA leadership on many important topics including the implementation of the revision of drug law and updated regulations, ICH implementation, and advanced therapy.

Learning Objectives

Discuss updates from CCDIE and NMPA leadership.

Chair

Ling Su, PhD

Speaker

New Progress of New Drug Evaluation
Fan Zhang, MS

Pre-Approval Inspection in China: Its Evolution and Key Points of Evaluation Principles
Yi Cao, MS

Pre-Approval Inspection in China: Its Evolution and Key Points of Evaluation Principles
Tiewei Zhai


Speakers
avatar for Ling Su

Ling Su

Research Fellow, Shenyang Pharmaceutical University Yeehong Business School, China
Dr. Ling Su is a Research Fellow in Shengyang Pharmaceutical University Yeehong Business School and a Venture Partner in Lilly Asia Ventures (LAV). He has 30 years of experience in drug regulatory and development. He had worked in various R&D management positions in the pharma industry... Read More →
avatar for Yi Cao

Yi Cao

Deputy Division Director, Div 4, Center for Food and Drug Inspection (CFDI)
Mr. Cao is mainly responsible for pre-approval inspection and overseas GMP inspection. Before joined in CFDI, he worked at Beijing Institute for Drug Control for 5 years
TZ

Tiewei Zhai

Deputy Division Director, Inspection Division 4, Center for Food and Drug Inspection (CFDI)
avatar for Fan Zhang

Fan Zhang

Project Manager, Center for Drug Evaluation (CDE), National Medical Products Administration (NMPA)
Ms. Zhang graduated from Long Island University and holds Master degree of Pharmacology and toxicology.

Thursday June 18, 2020 5:00pm - 6:00pm EDT
TBD Virtual Event Horsham, PA 19044
  09: Regulatory, Forum