Powering modern trials with eCOA platform solutions
Discover the future of clinical research with eCOA solutions that streamline data collection, improve adherence, and deliver actionable insights—all powered by our comprehensive decentralized clinical trial (DCT) platform.
Unified clinical trial solutions including eCOA, eConsent, remote monitoring, and connected sensors
eCOA for seamless data collection and oversight
Leverage electronic Clinical Outcome Assessment (eCOA) for accurate, real-time patient-reported data. Simplify workflows, reduce errors, and accelerate your trial timelines. Explore eCOA Solutions →
Take control of your trial
Incorporate eCOA with our advanced DCT features like remote data collection, study notifications, participant reminders, and real-time reporting, and Medable Studio and AI.
Unified clinical trial platform for modern research
From onboarding participants to data visualization, our platform delivers the flexibility and efficiency you need for today’s clinical research demands.
The Medable Effect
ROI for Phase III trials*
Rated DCT platform
Top Pharma customers
What makes us different
Best-in-class user experience
Informed by DCT experts, patient insights, and site feedback, the Medable platform accommodates the complex research landscape in an intuitive and simple user interface.
Designed to scale
Offered in over 60 countries and 120 languages, our cloud-agnostic, single API platform offers self-service build and a library of system integrations for maximum reach and scalability.
Extensive DCT network
Your study benefits from our extensive network of partners from retail pharmacy and site networks, data providers for RWE and LTFU, and direct-to-patient offering of connected sensors and home health providers.
Trusted by
The latest from Medable
Why cloud-based eCOA software is becoming the industry standard
The landscape of clinical trials is evolving rapidly, and at the forefront of this transformation is eCOA (electronic Clinical Outcome Assessment) software. This technology is streamlining data collection, enhancing patient compliance, and ensuring regulatory adherence like never before.
Medable Studio Showcase
More than an eCOA builder, Medable Studio’s simple point and click interface brings total control and transparency to the study launch process.
Demo On Demand: eCOA+, patient & site experiences, and pulse oximeter sensor
VP of Solution Consulting, Jess Dolphi, showcases a few of the platform’s features, including site experience, patient experience, data and oversight dashboards, and a demonstration of connecting a pulse oximeter sensor for remote data capture.
Medable Launches Partner Program for Faster Clinical Trial Startup, Greater Control, and Transparent Pricing
Medable unveils its new Partner Program, designed to empower contract research organizations (CROs) and other partners with generative AI-driven, self-service eCOA build capabilities for digitally enabled clinical trials.
Medable Introduces Long-Term Follow-Up Model for Cell & Gene Therapy (CGT) Trials to Reduce Costs and Improve Patient Access
Medable unveils its digital-first, Long-Term Follow-Up (LTFU) model for cell and gene therapy (CGT) trials. Medable’s platform reduces the burden on patients and sites involved in complex CGT trials and enhances scientific integrity with sustainable data capture across the FDA-required 15-year follow-up period for certain CGTs, including those using genome-editing techniques.
New Data Reveals DCT Components Linked to Improvements in Clinical Trial Access Among Underrepresented Communities
Medable's groundbreaking study with the Tufts PACT Consortium highlights the transformative impact of decentralized clinical trials (DCTs) on diversity.