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Wednesday, June 29 • 4:00pm - 5:00pm
#368: Conducting Trials in China

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Limited Capacity seats available

Component Type: Session
Level: Intermediate
CE: CME 1.00; IACET 1.00; RN 1.00

This session will describe some of the unique challenges with conducting clinical trials in China. We will describe approaches and challenges with the application of good clinical practices and include information on how risk-based analyses can be used to select appropriate sites for further review and potential audit.

Learning Objectives

Describe approaches and challenges with application of GCPs in China; Identify how risk-based analyses can be used to select appropriate sites for further review and potential audit.


Daniel Liu, PhD, MSc


Overview of Steps to Doing a Clinical Trial in China
Daniel Liu, PhD, MSc

Risk-Based Monitoring and Enrollment Pattern Analysis: Efficient Approaches for the Assessment Required by CFDA
Wenjun Bao, PhD

Update on Clinical Trials in China
Carol Zhu, MBA

avatar for Daniel Liu

Daniel Liu

Chairman, Chief Scientific Officer/Co-founder, Beijing Clinical Service Center
20 years in the pharmaceutical industry in the management of global clinical trials. A core expert in the Steering Committee of State Clinical Data Standardization, CDE CFDA; Associate Director of CDM China; Professor at CFDA Inst of Executive Development; Writer- in- chief of "Clinical... Read More →

avatar for Wenjun Bao

Wenjun Bao

Chief Scientist and R&D Manager, JMP Life Sciences, SAS Institute Inc.
Dr. Wenjun Bao is a Chief Scientist and R&D manager for JMP Life Sciences of SAS Institute Inc. She has rich experiences in clinical, biochemistry, molecular biology and bioinformatics researches. She has been a research grant review committee member for NIH since 2005 and research... Read More →
avatar for Carol Zhu

Carol Zhu

Senior Vice President and Managing Director, DIA China

Wednesday June 29, 2016 4:00pm - 5:00pm
201A Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA