From Protocol to EDC in Minutes: How AI Is Rewriting Study Start-Up

See how automated EDC database setup from a PDF protocol is reducing timelines, simplifying amendments, and reshaping the data manager’s role.

24

March

  • 3PM London / 10AM New York
  • Free
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Why attend?

Study start-up remains one of the biggest bottlenecks in clinical trials, with manual EDC database setup consuming time, effort, and resources. This webinar shows how AI is changing that process.

Attendees will see a live demo of a tool that takes a PDF protocol and automatically generates an EDC database setup. By translating protocol content directly into structured EDC components, the approach drastically reduces build timelines and improves alignment between protocol intent and data capture.

The session also explores the impact on protocol amendments, showing how automated protocol-to-EDC workflows enable faster updates, less rework, and greater agility when studies change.

Finally, we’ll discuss what this shift means for data managers: how their role evolves from manual configuration to oversight, validation, and design governance, and how teams can prepare to adopt AI-driven database build with confidence and control.

  • See how AI changes EDC database setup
  • Understand the impact on data management processes
  • Learn how to build confidence with AI
  • Assess the impact on the data manager role

Speakers

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Sylvain Berthelot
VP, Strategy & Marketing. CRScube

Sylvain has dedicated his 21-year long carrier on providing software for the pharmaceutical industry. He specialized in clinical trials 16 years ago, working at various eClinical technology vendors. His path has taken him to many conference and webinar stages, where he consistently strives to make the audience think differently about the topic of focus. Sylvain is passionate about implementing solutions that increase the efficiency of all involved in a clinical trial. He is now the Vice President of Strategy and Marketing at CRScube, where he embraces the company’s goal to make clinical trials accessible to everyone. He also dedicates a lot of his time to patient advocacy, increasing awareness about health conditions through his podcast On One Condition.

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