Medable delivers digitally enabled and data-driven clinical trials

Medable is enabling therapies to get to people who need them faster by providing technology that enables patients, providers, CROs, and sponsors to work as a clinical trial team.

Medable for Life
Science Enterprise

Our end-to-end (E2E) cloud platform provides a unified but flexible suite of tools where patients, providers, CROs and sponsors can work together as a clinical trial team. Use individual modules to meet the needs of your protocol, or leverage the entire platform to realize the full benefits of Medable’s E2E solution.

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Open APIs to work with third parties (EDC, EMR, IRT, etc)


eSource, eCOA, ePro, eConsent


User-friendly, role-based apps for each member of the clinical trial team


Automated workflows for clinical and business operations


Analytics and AI for algorithm development to automate workflows


Aggregated intelligence across multiple studies - consolidated, seamless clinical trial data insights and analysis capabilities

Medable for Patients

Engage patients and enable in-home clinical trials with registration, screening, consent and remote surveys and instruments.

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Medable for Sites

Empower your sites with easy to use apps that eliminate redundant data entry, enable better clinical care, and capture high quality data.

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Medable for data insights

Use machine learning to bring intelligence to data collected from patients, devices, sites and integrated systems like EMRs, third-party APIs, imaging centers and central labs.

Our Capabilities

Medable’s technology is currently being used by over 750,000 patients across 5 continents. We are the only enterprise cloud purpose built for life sciences with dedicated AI and machine learning. We have experience with registry studies and Phase I-IV clinical trials as well as in the following areas and more.

  • eConsent
  • ePRO
  • eCOA
  • eSource
  • Connected Devices
  • Patient Engagement
  • Global Device Provisioning
  • Multi-language
  • Data Management and Reporting
  • 21 CFR Part 11 Compliance
  • Hybrid Trials
  • Direct to Patient
  • Virtual Trials
  • Software as a Medical Device