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TransCelerate is helping to drive adoption of the RBM approach aimed at improving clinical trial efficiencies. Central monitoring is part of an integrated strategy that includes both On-site and Off-site activities. Key to an effective central monitoring strategy is the use of technology. This webinar offers the participant the opportunity to benefit from the collective knowledge and experience of a group of data, process and technology experts that came together to define the technical needs to enable RBM.

Live Webinar

Date: Wednesday, October 29, 2014

Time: 9:30 - 11:00 AM EDT

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Learning Objectives

This webinar provides talking points and key insights into the following:

  • Describe briefly the TransCelerate RBM Methodology
  • Examine the people, process, and technology needs for effective central monitoring
  • Describe what’s needed for data collection, aggregation, analysis and documentation for RBM
  • Discuss the vision for RBM given additional technology advances
  • Resources and further information

Who Should Attend:

Pharmaceutical and Medical Device Industries

  • Clinical Operations
  • Quality Assurance
  • Quality Auditing
  • Data Management
  • Study Monitoring
  • Biostatistics

 

Webinar Presenters
Shelly Barnes
Senior Project Manager
Sanofi
Biography
 
Mark Travers
Global Head, Clinical Study Units
Sanofi
Biography
 
Tom Verish
Group Director, Global Development Operations
Bristol-Myers Squibb
Biography
 
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