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Nov 18, 2018 9:00 AM - Nov 19, 2018 5:30 PM

Good Documentation Practice in Clinical Trials – Current Practice and Lessons

Faculty

Daniel  Liu, PhD, MSc

Daniel Liu, PhD, MSc

President & CSO, Beijing Clinical Service Center, China

Daniel Liu, PhD, has served for more than two decades in global clinical research departments, in both management and operations, for such multinational drug companies as Novartis, Pfizer, Sanofi, Schering-Plough, Johnson & Johnson, and Medidata. Dr. Liu has served as Core Expert of the NMPA CDE clinical data standardization Committee, and as Vice Chairman of the China Clinical Trial Data Management Group, an advisory member of DIA China committee, and a part-time professor of the NMPA Institute of Exceutive Development, a part-time professor of China Pharmaceutical University. He has taught more than 60 clinical research courses at home and abroad. He earned his PhD from the University of Illinois School of Pharmacy.

HuaLong  Sun

HuaLong Sun

General Manager, Meta Clinical Technology Co.Ltd., China

Charles  Yan

Charles Yan

Vice President, Head of Clinical Data Science Center, Jiangsu Hengrui, China

Juan  Liu

Juan Liu

Global Clinical Auditor, Bayer Healthcare, China

Lixin  Jiang

Lixin Jiang

, National Centre for Cardiovascular Diseases (NCCD), China

Aqiu  Chen

Aqiu Chen

Manager, Pfizer, China

Wenjing  Wu

Wenjing Wu

Manager, Data Managment Department, , Astrazeneca, China

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