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.

Medable web interface showing translation management with summary of 7 locales and 14 assets, a status donut chart, automation suggestions for 13 assets and 7 locales, and a table listing participant activity translations across different language locales.

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

Medable dashboard showing summary update of clinical study enrollment and patient status with AI recommendation on drug supply, and CRA Assistant chat requesting overall study compliance and site delays.

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

Medable worldwide map

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The industry has accepted outdated UX for too long.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)

Medable clinical trial interface showing ovarian cancer study participant visits, training steps, and sponsor workspace selection.

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

"If all support teams worked like Medable, my job would be a dream!"
Site user
Top 10 Pharma Study
Animation of a digital form building interface showing a list of survey sections with preview buttons and a mobile preview of a symptom reporting screen with symptom options and navigation buttons.

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
Animated GIF showing white glowing orbs connecting with white lines on a dark purple background, forming a dynamic network pattern.

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.
Everest Group

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

Learn how Medable enabled a top-5 pharma to scale vaccine mega-trials with near-100% enrollment, real-time safety data, and >90% diary compliance.

Case study: Scaling global vaccine mega-trials for a top-5 pharma

Learn how Medable enabled a top-5 pharma to scale vaccine mega-trials with near-100% enrollment, real-time safety data, and >90% diary compliance.‍

PDF
Case study: Scaling global vaccine mega-trials for a top-5 pharma

The latest from Knowledge Centers

Blog posts

What happened at ASCO 26?

ASCO
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With 44,000+ oncology professionals in attendance, ASCO 2026 may have been the most consequential in recent years. From a standing ovation for pancreatic cancer to the first positive sarcoma trial in history, here's everything that mattered at Chicago's McCormick Place this week.

Blog posts

Real-time clinical trials are here. Medable was built for them.

Real-time clinical trials are here. Medable's continuous trial management platform gives sponsors the evidence generation, agentic AI, and regulatory-ready infrastructure to run clinical programs at the speed the FDA now expects.

Guides

Key criteria for evaluating AI and agentic AI clinical trial vendors

Artificial Intelligence is rapidly transforming clinical research. From patient recruitment and protocol design to medical writing and data review, AI-powered solutions are becoming embedded across the clinical development lifecycle. More recently, the emergence of Agentic AI (systems capable of planning, reasoning, and executing multi-step workflows with varying degrees of autonomy) has generated significant excitement throughout the industry.

However, not all AI solutions are created equal. While many vendors promise dramatic improvements in efficiency and productivity, clinical trial organizations operate in one of the most highly regulated environments in the world. Success depends not only on technical performance but also on compliance, validation, governance, security, and trust.

As sponsors, CROs, and technology teams evaluate potential AI partners, they need a framework that extends beyond traditional software procurement criteria. The following considerations can help organizations assess both AI and Agentic AI vendors and identify solutions that are truly ready for clinical research.

See how Agent Studio can transform your trials.