Drug Information Association Logo

Workshop4: Project Management in Clinical Data Management

May 11 2014 8:30AM - May 11 2014 5:30PM | Shanghai International Convention Center No. 2727, Riverside Avenue Pudong 200120 Shanghai China

« Back to Listing

Overview 

Clinical trial data include various sources, can be collected via paper or electronically, either way has advantages and disadvantages in data quality, operation, project budget control, et al. Selecting the most
suitable data collection approach, implementing well considered data quality control procedures and applying appropriate risk control via good project management, are extremely important for quality data collection starting from clinical trial planning stage to database lock. This one day workshop will discuss best approaches for EDC study related clinical data, central lab data, ePRO and IV/WRS quality data acquisition.

Who Should Attend 

  • Clinical trial data managers
  • Clinical trial project managers and administrators
  • Clinical trial monitors
  • Clinical trial quality assurance and quality control professionals
  • Clinical development professionals and study coordinators
  • Clinical regulatory affairs professionals

Learning Objectives 

  • To share view of di!erent data needs and challenges
  • To discussing best practices in project management during trial execution
  • To learning best approaches for EDC study related clinical data, central lab data, ePRO and IV/WRS quality data acquisition

Contact Information 

For general inquiries and registration, contact
Mr. Fei XIE
Phone +86.10.6260.2240
fei.xie@diachina.org or dia@diachina.org

For exhibiting, hosting, and advertising inquiries, contact
Ms. Jean XU
Phone: +86.10.5923.1096
jxu@kellencompany.com

To Register, click here.

Instructor(s) 

Previous Next
« Back to Listing Back To Top