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CROs and sponsors serious about driving clinical trial quality, efficiency, and oversight, are aware of the FDA guidance: “A Risk-Based Approach to Monitoring.” From a practical level, how do you start your program and gain the full advantages of RBM?

Key topics of discussion include:
  • Creating a sustainable RBM strategy with a common platform
  • Decreasing your site visits and increasing the efficiency of oversight
  • Focusing activities on preventing or mitigating risks
  • Leveraging risk insights to increase the quality of trial design

This webinar focuses on a CRO implementation of the PerkinElmer RBM Solution, powered by TIBCO® Spotfire®, including compelling lessons and surprising insights that continue to drive trial design enhancements and optimize the CRO-sponsor partnership.

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