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Agentic AI built for clinical development
The only agentic AI platform designed from the ground up for GxP-regulated environments. Model-agnostic. Human-in-the-loop. Connected to 15+ clinical and enterprise systems without replacing any of them.
- Full observability: Transparent, explainable, auditable decision trails
- Connected to your systems: Veeva, Oracle, Medidata, MS 365, Snowflake, and more
- GxP-ready by design: 21 CFR Part 11, Annex 11, ICH GCP, ALCOA+ audit trails
- Human-in-the-loop: Configurable oversight and escalation for every workflow
- Model-agnostic flexibility: Not locked into a single AI provider
Connects to the systems you already use
Over 30 secure, validated connectors to the systems you already run on, from Veeva, Oracle, and Medidata to Snowflake, BigQuery, and your collaboration stack. Your data stays where it lives. Medable just makes it work harder.
The first time I've seen agents in clinical ops this far advanced... you're really ahead of the pack.
Agentic capabilities across your entire trial
From monitoring to document management to study builds, agentic AI capabilities save you time and protect your data quality.
Platform features
Cloud agnostic API easily integrates data
Learn the fundamental approaches and best practices to create a seamless decentralized approach for clinical trials.
Notifications and reminders
Drive adherence and ensure patients stay engaged with built-in notifications and reminders.
Connectors
MCPs connect systems like EDC, TMF, IRT, and Teams so agents surface insights in Medable Agent Space and take action across your workflows and systems.
Ontology Layer
We normalize your data so agents can deliver insights and act instantly.
Multi-study Participant app
Patients can log into any new study with Medable’s participant app available on both Apple and Google app stores. Study teams mitigate app development and deployment time getting to FPI faster.
24/7 support
Medable offers 24/7 support for trial participants and sites with a 92% first call resolution ensures that help is only a click or call away.
Reporting and dashboards
Gain a quick snapshot of your trial’s status, or deep dive into the nuances of your sites and patients, now supported by Medable AI for faster analysis.
BYOD and Provisioned Devices
Give your sites and patients the convenience and comfort they deserve with BYOD, or our 99% on-time provisioned devices.
What our customers are saying
"Everything has been remarkably smooth, which is not always the case with eCOA vendors."
Top 10 Pharma
"When it comes to modern eCOA solutions Medable is leading the pack."
Director, eClinical Development, Top 5 CRO
"Medable offered robust early engagement and SME dialogue early in planning."
Director, DCT Sourcing, Top 5 Pharma
Platform accolades
A decade ago, our founders’ experiences in clinical research and life sciences drove them to create Medable, a simple cloud-based platform that could improve theconduct of trials. Over the last ten years, we’ve conducted nearly 400 trials on our platform, continually refining it to provide a better experience for sites, patients, and caregivers.Today, we’re excited to announce that our customers are entering a new era of control, ease of use, and simplicity.
The latest from Knowledge Centers
Scaling five oncology studies with one kickoff meeting
One kickoff. Five oncology studies. 50% less build effort, and a week ahead of schedule, even after a late protocol amendment. See how a shared foundation changed the way this sponsor runs oncology programs.
Which clinical trial workflows are realistic for AI Agents?
AI agents are moving from demos into day-to-day clinical operations, but not every workflow is a good fit. This guide explains which clinical trial workflows are realistic for AI agents today, from TMF filing to clinical monitoring, and where people still need to make the call.
Proactive consent review helps pediatric studies stay ahead of FPI
A top-5 pharma partnered with Medable on two pediatric vaccine studies in South Africa, where parents and guardians consent on behalf of their children. By reviewing consent materials from the caregiver’s perspective, Medable flagged inconsistencies early enough for the sponsor to revise the forms and secure IRB re-approval before first patient in.