How to balance scientific complexity and its inherent issues with patient-centric design of the protocol to help increase R&D efficiency in clinical trials.

Featuring:  Steven R. Cummings, MD, Emeritus Professor of Medicine, Epidemiology, and Biostatistics, University of California, San Francisco and Scott Chetham, PhD, CEO, Faro Health Inc. 

Abstract: In clinical trials, documents, data and applications are separate with no single source of truth. Imagine a world where a clinical trial protocol design can be done and implemented in days. This vision is becoming a reality with the use of smart templates to build trials and standards-based ontologies linking downstream systems while using data to build real-time patient journeys and budget insights.

What You Will Learn:

  • Learn how clinical study teams can balance the complexity of modern trial designs with a patient’s first mission
  • Discover innovative approaches to minimize patient burden and enhance site feasibility
  • Utilize data driven insights to proactively identify areas of decentralization during the initial design of the protocol
  • Discuss challenges and strategies for the current state of adoption of decentralized trials in research
  • Explore the role of modern trial designs and the collaboration done by digital clinical design platforms
  • Explore the role of collaborations in addressing common barriers in the research community
  • Defining patient-centricity in clinical trials

Watch Xtalks Webinar