Clinical trial software that puts you in control
A powerful, intuitive platform designed for seamless data collection, making participation easier for everyone.
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eCOA and digital measures
Offer participants better experience that drives adherence, while taking eCOA off the critical path to trial launch.
eConsent
Modernize your entire consenting process with a scalable eConsent management solution, preferred by participants and supported worldwide.
Medable Studio
More than a builder, Medable Studio with Medable AI delivers unprecedented control and transparency over study creation and launch.
Therapeutic area pathways
Deploy quickly and easily across 100+ indications, with specialization in Oncology, Weight management, Vaccine, Cardiology, Dermatology, Endocrinology, Immunology, and more.
“Use of the platform was incredibly straightforward and their training demo modules made it easy for our organization to implement.”
Associate Chief Medical Officer & SVP of Clinical Research and Medical Affairs, U.S. Renal Care
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 adherenceand ensure patients stay engaged with built-in notifications and reminders.
Patient caregiver and site networks
Experience a platform informed directly by user experience and recommendations of patients, caregivers, and clinical trial sites.
Digital measures, connected sensors, and wearables
Standardize integrations and capture digital physiological measures across a variety of therapeutic areas.
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 an 80% 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.
Unified integration enables you to effortlessly connect your entire workflow
The Medable platform is built specifically to ensure a seamless digital data flow across your studies and portfolio of clinical trials. As aground-up, interoperable platform, there are a range of options for how the Medable platform and data can integrate with your broader technology ecosystem with a range of options for all variations of EDC, IRT, CDB etc depending on whether data are pushed via transfers or pulled via API.
Studies delivered
100%
On time go-live
Quality
90%
eCOA adherence for 8 of 10 studies
Support
92%
First contact resolution
Device delivery
98%
Devices shipped on time
With the eConsent market expected to continue its ascent over the next ten years, it’s apparent to those who have used it that the “e” in eConsent stands for much more than electronic. Analysis and real-world examples show that it can be efficient, educational, and empathetic, leading to better participant education, reduced participant dropout, lower administrative burden for sites, reduced audit findings, and more.
Experience the award-winning platform designed for sponsors, sites, and participants.
