Global Strategies for Clinical Research Information
Webinar Series



AMIA is pleased to continue its support of an e-learning webcast series on Global Strategies for Clinical Research Information. This series is a "one-stop-shop" for all those in the Pharmaceutical and Healthcare industries to acquire up-to-date information on the many facets and faces of the industry's adoption of clinical data standards.

From overviews, updates and futures to detailed lessons learned, you will hear from thought leaders and implementers who are at the front of the standards movement.

Please join us for the entire series or for the individual sessions that align with your personal interests.

The Global Strategies for Clinical Trial Information series is offered by BetterManagement and sponsored by CDISC and AMIA, you can be sure that the information is timely and will be thoughtfully presented.

Click here for more information on the webcast series

Upcoming Webcasts:

Using CDISC Standards to Address Information Sharing and Interoperability Needs of Academic Research Centers
October 12, 2007

See the Abstracts for the Expo (pdf)

Click here for more information (MS Word)

• Session 1: WHO International Clinical Trial Registry Platform - What is the Value of Registering?
  Presented By: Ed Helton, PhD, SAS; and Ida Sim, MD, PhD, World Health Organization
  View archived webcast now
  
  
• Session 2: Harmonizing CDISC Submission Models - SDTM and ADaM
  Presented By: Ed Helton, SAS; Cathy Barrows, GlaxoSmithKline; Musa Nsereko, Cephalon; and Greg Anglin, Eli Lilly Canada
  View archived webcast now
  
  
• Session 3: The Global Trial Bank - Meeting the Needs of the International Biopharm Community and the Patients it Serves
  Presented By: Don Detmer, MD, American Medical Informatics Association
  View archived webcast now
  
  
• Session 4: Why Clinical Development Teams Should Care about Data Standards - Part I: An Introduction to the CDISC Operational Data Model (ODM)
  Presented By: Ed Helton, SAS; Sally Cassells, Lincoln Technologies; and Dave Iberson-Hurst, Assero Limited
  View archived webcast now
  
  
• Session 5: Why Clinical Development Teams Should Care about Data Standards - Part II: The Inner Workings of the ODM
  Presented By: Ed Helton, SAS; Sally Cassells, Lincoln Technologies; and Dave Iberson-Hurst, Assero Limited
  Thursday, May 18, 2006
  11:30am - 12:30pm EST
  
  
• Session 6: Why Clinical Development Teams Should Care about Data Standards - Part III: Real World Experiences with the ODM
  Presented By: Ed Helton, SAS; and Gary Walker, Quintiles
  Thursday, June 8, 2006
  11:30am - 12:30pm EST
  
  
• Session 7: The Biomedical Research Integrated Domain Group (BRIDG) Model
  Wednesday, July 26, 2006
  11:30am - 12:30pm EST
  
  
• Session 8: Update on the CDISC Business Case for Industry Data Standards
  Wednesday, August 16, 2006
  11:30am - 12:30pm EST