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Who Should Listen:  Trial sponsors, clinicians, medical device developers, and site personnel looking to monitor complex processes with minimal error, fewer resources, and lower costs.

What You'll Learn:  Join our panel of experts for this roundtable discussion to learn more about how the use of a technology-amplified, real-time, risk-based "just-in-time," approach to monitoring can help you:

  • Ensure integrity of trial data and patient safety
  • Optimize trial efficiency and quality
  • Streamline sponsor, CRO, and trial site team interaction

Presenters:

  • Marie Hanley 
    Vice President, Global Quality Services, Clinipace Worldwide
  • Monika Frey
    Vice President of Global Clinical Operations, Clinipace Worldwide
  • John C. Parnell, RPh, MHA
    Director, Global Clinical Monitoring, Clinipace Worldwide
  • Deborah Rosenfelder
    Clinical Trials Manager, Clinipace Worldwide

Free Webcast:

Mitigating the Challenges of Clinical Trial Monitoring: A Technology Amplified Approach

Watch the webcast today!

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