18-19 March 2010
Philadelphia, PA, US

Pharmaceutical and biotech companies are increasingly looking to clinical trial management systems (CTMS) to help streamline their clinical development operations. While a CTMS can effectively manage and track the results of multiple ongoing trials with access to real-time project information through a centralised database, the challenges associated with implementing and managing a CTMS are significant given the complexity of the technology and broad range of information being collected and tracked.

Building on a successful two-year history, this programme continues to serve as an excellent platform for industry discussion and collaboration among various CTMS stakeholders. This programme addresses the challenges of integrating CTMS systems both within the organisation across various other clinical systems as well as with external systems. Don’t miss this opportunity to hear in-depth industry case studies and learn from the challenges and successes of other companies.  

This conference continues to provide the only focused forum for discussion regarding CTMS systems.  

Top five reasons to attend:

• Hear a case study on the internal integration of CTMS, IVRS and Other Data Sources
• Assess strategies for interfacing and obtaining data from CROs
• Gain insight on lessons learned and success stories from embedding CTMS into the organization
• Hear best practices for validation of CTMS systems
• Discuss the impact of EHR on paving the way for CTMS efficiencies