Reducing the time to “First Patient In” remains a challenge, as manual study builds create persistent bottlenecks.
Join Paul O’Donohoe, Senior Director, eCOA Product and Science, Angela May, Senior Consultant, Medidata, and a global pharma expert, as they examine the implementation of next generation eCOA today. This session details how automation, anchored by human expertise, can power fast and high-quality eCOA study builds.
Attendees will learn how to:
- Convert protocols directly into baseline eCOA builds to replace weeks of manual specification.
- Reduce build effort by up to 50% to improve quality and accelerate “First Patient In” dates.
- Leverage smart form recommendations and imports from libraries to remove repetitive build work and safeguard instrument validity.
- Combine AI automation with expert oversight to mitigate regulatory risk and ensure compliance.
- Discover how integrating AI transforms operational efficiency into a competitive advantage, ensuring data quality and a seamless start for your patients.
Join us to discover how operational efficiency builds a more predictable path to First Patient In.