Where experience meets evidence.

Reach more participants, generate high-quality data, and simplify clinical trials, with a unified, easy-to-use platform.

One platform, from start to finish.

Onboard your participants

Total Consent Management incorporates easy-to-use tools like TeleVisit, remote scheduling, and compliant wet and dry signature to get your study started quickly and smoothly.

Take control of your trial

Keep your study on track and generate high-quality evidence with robust features like remote data collection, study notifications, participant reminders, and real-time reporting.

Data reporting and visualization

Oversight of your study data at your fingertips.

The Medable Effect


ROI for Phase III trials*


Rated DCT platform

14 of 20

Top Pharma customers

What makes us different

Medable platform morning dose diary

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.

Medable worldwide map
Medable site data collection dashboard

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

White Papers, Case Studies, Reports

U.S. Renal Care achieves 75% site adoption of eConsent with Medable

Medable’s Total Consent, used by U.S. Renal Care in top ten pharma-sponsored study, proved to be a flexible, fast, and efficient solution for the elderly renal care population.


Ethical Review of Decentralized Clinical Trials (DCTs): Tools, Resources & Best Practices

6 min

Industry experts from Medable and Harvard School of Medicine discuss how to equip your future digital/decentralized trial IRB & ethics submissions for success.

Blog posts

Rapid evolution: How DCT’s DNA became standard in modern clinical trials

It’s impossible to deny how different clinical trials look almost four years after the pandemic revolutionized clinical research. Today, the digital and decentralized tools and technologies that enabled clinical trials to carry on through the COVID-19 pandemic are present (in some form) in nearly all clinical trials, a far cry from the dynamics of 2019.

Elderly Patients in US Renal Care Trial using Total Consent

Medable Achieves 75% eConsent Adoption Across Elderly Patients in Pivotal U.S. Renal Care Clinical Trial

6 min

The Phase IV trial, funded by a top-10 global pharmaceutical company, had a narrow recruitment window to enroll patients suffering from Anemia in End Stage Kidney Disease (ESKD) across more than 40 dialysis centers, involving 476 site users.

Medable Prix Galien Award Best Digital Health Solution

Medable Wins 2023 Prix Galien Award for Best Digital Health Solution

6 min

Medable was awarded ‘Best Digital Health Solution’ from a field of 24 nominees at the Prix Galien USA Forum in New York City. This recognition underscores the impact of Medable’s evidence generation platform on clinical research worldwide.


Medable Partners with Pluto Health to Optimize Patient Experience and Improve Access to Clinical Trials

6 min

This strategic partnership combines best-in-class patient care coordination service and clinical trialsplatform to streamline execution, improve data quality, and enhance patient experience.

See how Medable can make your trials more efficient.