Medable Clinical Trial Platform (Agentic AI, eCOA, and DCT solutions)

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Clinical development, meet agentic AI.

A new model for clinical development is taking shape where startup, enrollment, and conduct move in days and months, not years. One platform. Unified workflows, data, and clinical context. Get the full power of agentic AI across the full trial lifecycle at your fingertips.

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Unlock the agentic advantage

Unify your clinical systems and workflows, and turn data into intelligent, trusted action while reducing manual burden across clinical operations.

Medable’s Agent Platform is purpose-built for clinical development, with deep context across GxP compliance, regulatory requirements, and the operational complexity that general-purpose AI platforms aren't equipped to navigate.

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Less risk. More control. eCOA, reimagined.

Medable's agentified eCOA brings AI-powered workflows to every stage of the trial — from build and deployment to study conduct and data review — delivering consistent, high-quality data and stronger participant adherence.

Spanning eConsent, sensors, provisioned devices, and BYOD, Medable offers a unified experience that reduces operational complexity across every touchpoint of the trial.

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Clinical outcomes backed by real-world evidence

90%+ eCOA participant adherence

Near-perfect compliance across a 70+ site master protocol.

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43% Reduction in translation timelines

Half the time to go-live with AI-powered translation.

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1 day Trial build time

From weeks to one business day with Medable Studio.

Case Study

99% eCOA adherence in Japan

FPI achieved ahead of schedule across a complex regional rollout.

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Trusted, traceable, GxP-ready AI

Autonomous where it can be, human-led where it must be. Clinical judgment, amplified, never replaced.

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Built for global regulatory compliance and data integrity

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Medable's 1:1:1 vision

1 day study start, 1 day patient enrollment, 1 year study conduct.

An ambitious vision and one Medable is actively building toward. With agentic AI purpose-built for clinical development, we're making meaningful progress toward timelines the industry once thought were out of reach.

The clinical monitoring agent gives us a holistic view, but what really matters is the site. Normally, we find out about enrollments or screen failures through hundreds of emails, easy to miss. Having that site-specific data right when we log in is a real game changer.

Clinical Research Associate

Top 10 Pharma

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