This presentation was delivered by Andrew Taylor, Head of Asia-Pacific Clinical Data Management, Roche at BioPharma Asia 2013.
The presentation focuses on:
â¢Technical Guidelines for Data Management in Clinical Trials (SFDA, CDE)
â¢The development of a China office as part of a global Pharma data management function
â¢Leveraging global resources, systems & processes to accelerate the growth & competence of the China office
â¢Utilization of talent in Asia to support global drug development
â¢The collaboration of global and regional staff to support clinical trials to accelerate drug registration in China
If you are interested in this presentation then you may also be interested in The BioPharma Asia Convention 2014. Click here to visit the website