Protocol design can have a significant impact on patient engagement and clinical trial performance. In this live webinar, explore the findings of a recent scholarly study conducted by the Center for the Study of Drug Development (CSDD) at Tufts University School of Medicine which characterize current protocol design practices and their effects on study volunteer experience and clinical trial performance.

Join Ken Getz, Director of Sponsored Research Programs & Associate Professor at Tufts CSDD, in a live session on Tuesday, March 19, 2019 at 1pm EDT to learn how small, medium, and large organizations can implement new practices to:

• Optimize patient engagement
• Reduce clinical trial costs
• Accelerate clinical trial timelines

The discussion will cover an array of topics such as: Aenchmarks on industry-funded clinical trial protocol scope and structure; overall and study-specific study timelines; patient recruitment and retention rates; study volunteer participation experience; and new practices in protocol design.

This webinar will be suitable for data managers, clinical trial site managers and ClinOps professionals from CROs, early-phase pharma, medical device companies and diagnostics companies.

For more information or to register for this event, visit Maximizing Clinical Trial Performance Using New Protocol Design Practices.

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Contact:
Candice Tang
Tel: +1 (416) 977-6555 ext 400
Email: ctang@xtalks.com