Already a DIA Member? Sign in. Not a member? Join.

Sign in

Forgot User ID? or Forgot Password?

Not a Member?

Create Account and Join

Shanghai International Convention Center

May 24, 2015 8:30 AM - May 27, 2015 5:00 PM

No. 2727, Riverside Avenue, Pudong, 200120 Shanghai, China

The 7th DIA China Annual Meeting

Session 0302 The Feasibility of Initiating Clinical Trials by Single IRB Approving in China

Session Chair(s)

Shuting  Li, MD

Shuting Li, MD

Deputy Director

GCP Alliance, China, China

Speaker(s)

George  Guo

George Guo

Novartis Pharmaceuticals, China

Global Monitoring Operation Country Head

Winnie  Xu

Winnie Xu

Quintiles Medical Development (Shanghai) Co. Ltd, China

AD

Huanling  Wang

Huanling Wang

Peking Union Medical College Hospital, China

Vice Director, Clinical Pharmacology Research Center

YongChuan  Chen

What will be reviewed in multicenter ethical review units should review what?

YongChuan Chen

Xinan Hospital of Army Medical University, China

Director,Drug Clinical Trial Institute Office

Zhiqiang  Ning

Zhiqiang Ning

Shenzhen Chipscreen Biosciences, Ltd., China

Vice President, Research & Clinical Development

Tim  Shi

The feasibility of center ethical review implementation in China

Tim Shi

GlobalMD, United States

Executive Director

Have an account?

Be informed and stay engaged.

Don't miss an opportunity - join our mailing list to stay up to date on DIA insights and events.