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Enhance Process and System Interopability to Optimize Data Quality, Improve Trial Efficiency and Ensure Protection of Human Subjects

November 13-14, 2019
  • Philadelphia, PA

The concept of RBM is nothing new, however many questions still remain around successfully achieving implementation and adaptation: Are we making it more complex than it needs to be? How can we work more effectively with sites and other stakeholders? How can we demystify and implement complex RBM models in a straightforward manner? And now, with each organization collecting clinical data across multiple systems, usually in their own format and reporting environments, the integration of data has become increasingly difficult.

CBI’s Risk-Based Trial Management and Monitoring conference is dedicated to reducing the complexity of implementing an efficient RBM methodology and refining processes while providing real-world strategies to system adoption and process integration.

Key Discussions Include:

  • Deconstruct the complexities of RBM
  • Prepare for audits and inspections in RBM programs
  • Discuss key factors in establishing thresholds
  • Explore TransCelerates approaches for an efficient and
    effective RBM process
  • Determine tools that can support central monitoring

Previous Attendee Acclaim:

My company is just starting to implement RBM.
This conference helped me understand A-Z all the
details that will be needed – exciting!

Senior CRA, Regeneron

The ideal forum to be on the forefront of emerging strategies and approaches to clinical trial oversight.

Manager, Clinical Monitoring, St. Jude Medical

Great conference – nice broad array of attendees from different side of the business – gives good perspective.

Information Strategist, Pfizer

This conference was a great way to get the pulse of RBM across the industry and prepare for the next steps as it evolves.

Associate Director, Clinical Innovation, INC Research