PSI CRO Slashes Clinical Trial Site Identification Time from Weeks to Minutes with Arango AI
Event summary
- PSI CRO reduced clinical trial site identification from up to six weeks to minutes using SYNETIC™, an AI-enabled knowledge engine powered by Arango's Contextual Data Platform.
- SYNETIC™ unifies fragmented clinical research data into a trusted contextual data layer, improving site selection efficiency and reducing costs.
- The solution addresses the industry challenge where 30-40% of clinical trial sites under-enroll and ~15% never enroll a single patient.
- SYNETIC™ provides explainable AI insights, including rationale behind site recommendations, supporting evidence, and confidence levels for predictions.
The big picture
The clinical trial industry faces persistent inefficiencies, with operational costs exceeding $160 per minute and millions of dollars lost due to underperforming sites. PSI CRO's success with SYNETIC™ highlights the growing importance of contextual data infrastructure in enabling AI-driven decision-making. This trend is part of a broader shift towards data unification and explainable AI in complex, regulated industries.
What we're watching
- AI Adoption
- How the pace of AI adoption in clinical research will affect trial timelines and costs.
- Data Integration
- Whether other clinical research organizations will follow PSI's lead in unifying fragmented data for AI-driven decision-making.
- Regulatory Compliance
- The extent to which explainable AI will become a standard requirement in regulated healthcare environments.
