The agentic platform built for science

The stack that powers your study lifecycle, from a single build to your entire portfolio, with control and quality.

Everything you need to build, manage, and oversee trials

• Unified orchestrated platform: eCOA, eConsent, TeleVisit, devices, and agents all in one login, with one view
• Connects to all your systems: Make sense across your clinical systems with an agentic ontology layer and MCP connectors
• Real-time visibility from day one: See what patients and sites see during the build not weeks later
• Agentic AI built for GxP: Purpose-built agents with human-in-the-loop oversight and full audit trails
• Portfolio value that compounds: 50% faster builds with reuse. ~80 hours saved per study
• Global scale, local precision: 80+ countries, 120+ locales, 400+ validated instruments
• Compliance by design: 21 CFR Part 11, Annex 11, HIPAA, GDPR, ICH GCP, and more

Three pillars. One platform. Zero fragmentation.

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Agentic eCOA & evidence collection

AI-powered Study Studio is a no-code visual builder with 400+ validated instruments. Studies that used to take 16-20 weeks go live in 4-6 weeks-- some go live in a day.

Instrument Generator · Translation Workbench · Visual builder

Agentic clinical development

AI agents support your clinical trial lifecycle, proactively monitoring, flagging risks, and recommending actions across your CTMS, EDC, and eTMF with human-in-the-loop oversight.

Clinical Monitoring Agent · TMF Agent · PI Summary Agent

Device logistics management

Procurement, provisioning, and delivery from six global depots, platform agnostic, with one all-inclusive monthly rate.

99% on-time delivery · 65+ countries · 50,000+ devices shipped

Technology that people actually want to use

The industry has accepted outdated UX for too long. Every screen on Medable's platform experience is designed with input from our Patient, Caregiver, and Site Network (PCN) to drive the highest possible adherence and satisfaction.

Designed for real lives, not just protocols

Built with ePROs, ObsROs, eConsent, and TeleVisits, including dedicated schedules and activities for caregivers, unlock a user-friendly patient experience.

90% app satisfaction · 99.27% adherence · 97% retention (10yr LTFU)

Everything a site needs, nothing they don't

Sites become advocates with real-time dashboards, single sign-on, and training that's done before FPI, not scrambled together after.

90% first contact resolution · 90% site adherence on assessment and eligibility tasks

See what you're building, instantly

No more sending requirements to a vendor and waiting weeks. Study Studio is a collaborative, no-code workspace where you design, preview, and iterate in real time.

35x faster builds · 200+ hours saved/study

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.

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.

Clinical monitoring

Real-time site monitoring across CTMS, EDC, and RBQM. Surfaces risk signals. Recommends actions.

Trial master file

Automated document tagging, classification, and filing across languages. Built-in QC.

Investigator review

AI-assisted data synthesis, change detection, and 21 CFR-compliant e-signature support.

Instruments & translations

AI-driven eCOA generation from protocol or source instruments, with clinical-grade translation standardized to scale.

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