Clinical trial teams continue to struggle with fragmented processes across sites, sponsors, and contract research organizations. Documents, milestones, and study data often reside in disconnected systems, creating duplication, delays, compliance risks, and increased administrative burden.

This session will explore how organizations could build artificial intelligence (AI)-connected clinical ecosystems through the integration of site and sponsor technologies, including electronic investigator site files, electronic trial master files, and clinical trial management systems. Using real-world implementation examples and lessons learned, attendees will examine practical integration models, governance considerations, and change management strategies that improve collaboration, streamline document exchange, enhance inspection readiness, and reduce operational inefficiencies.

Attendees will leave with actionable approaches to evaluate integration opportunities within their own organizations and strengthen sponsor-site partnerships throughout the study lifecycle.

CEU: 1.0 ACRP

Speaker:

• Guillaume Gerard, Chief Operating Officer, Agatha Inc