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Event Overview

Event Overview

Experts from sponsor companies, CROs, investigative sites, and e-clinical service providers come together to share strategies that address the full spectrum of the most important EDC issues BEYOND just data capture including:
  • Integrating multiple platforms
  • Engaging sites
  • Reducing redundancies
  • Implementing new standards
  • Incorporating safety reporting

  • Do you want to discover ways to integrate several e-clinical technologies into one seamless system for faster study completion?
  • Are you prepared to coordinate your e-clinical technologies with the latest industry standardization initiatives?
  • Are you actively engaging clinical site preferences for more effective participation outcomes?
  • Have you explored the true value of e-clinical beyond data capture?

IIR’s 13th annual EDC & Beyond event brings together experts from sponsor companies, CROs, investigative sites and e-clinical service providers to put the “beyond” into your e-clinical systems, addressing the full e-clinical spectrum of technology and usage for optimal synergistic performance.


2008 Presentations
Creating a CRO-centric Clinical Trial Management System (CTMS) Focusing on Standards for Data Exchange
Charlie Dougherty Director, R&D IT SHIRE PHARMACEUTICALS
Scott Johnson Associate Director, Clinical Application Support (CAS) ICON CLINICAL RESEARCH
Jennifer Vineyard Senior Clinical Project Manager ICON CLINICAL RESEARCH
Practical Implementation of CDISC for Meta and Clinical Data Interchange
Neil Vivian MSc, BSc, VP Technology Solutions ERESEARCH TECHNOLOGY

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