Live Webinar
Years of clinical trials, yet most of the data has never been reused. Each clinical study generates rich patient-level data. Once a study closes, the majority of that data remains locked inside trial data management systems, effectively invisible to the rest of the organization. It is siloed by study, system, and therapeutic area, with governance processes built for single use rather than reuse.
There's a better architecture.
In this webinar, we'll give you the practical steps needed to make clinical data available for internal evidence generation without compromising patient privacy, regulatory compliance, or data integrity. We'll walk through a real pharma deployment of DISQOVER's semantic layer and knowledge graph, showing you exactly what each step looks like in practice.
We'll cover the architecture, the governance mechanics, and the real-world results, including how AI agents could operate via MCP, and be governed by the same rules as human researchers, by design.
Responsible for access policy, regulatory compliance, and data stewardship across clinical data environments
Designing data platforms that need to support reuse, federation, and governed access at scale
Building AI capabilities on top of regulated clinical data and navigating governance in an agentic world
Product Director
ONTOFORCE
Solution Enablement Director
ONTOFORCE
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