Medable eCOA

You remember Medable, you won’t recognize our eCOA

While you’ve been away, we’ve rebuilt eCOA from study setup to the participant experience. Studio, AI, and automation make it easier to launch studies, manage changes, and keep participants on track with results from global studies to back it up.

We handle the complexity, you keep control

Complex protocols shouldn’t create complex operations. Medable absorbs more of the complexity behind eCOA so study teams can move faster while maintaining control and regulatory quality.

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Start sooner and keep studies on track

Build and launch globally, faster

AI-powered design, translation, validation, and deployment now run in parallel, enabling near-simultaneous multi-country deployment.

Change without the chaos

Handle protocol amendments, cohort changes, and other mid-study updates without turning every change into a major rebuild.

Keep the data coming

Real-time data and dashboards help teams spot missed entries, while notifications and reminders keep participants on track, with daily diary adherence of 90–97% demonstrated across global studies.

See how far eCOA has come

Your next study deserves more than legacy eCOA. Before you go with the familiar, see what you could be missing.

Old eCOA model

Medable eCOA model

Build, review, translate, validate. One step after another
Design, translate, validate, and deploy in parallel with AI-Powered Study Studio
English first. Then country-by-country rollout
Near-simultaneous global go-live, cutting 10–20 weeks from country activation
eCOA build takes weeks or months. FPI waits
Build and deploy in as few as 4 weeks
Low adherence becomes another problem for sites to solve
>90% daily diary adherence, protecting the quality of your study data
When it comes to modern eCOA solutions Medable is leading the pack.
Director
eClinical Development, Top 5 CRO

Results with top customers at programmatic scale

35x

faster builds compared with legacy eCOA

90%+

participant adherence across studies

2,100+

accommodated on one global program

A lot has changed since you last used Medable

  • Agentic instrument configuration
  • AI-powered translation
  • AI-assisted pre-testing and quality engineering
  • Data on demand
  • Standardized deployment
  • Agentic PI summarization
  • Episodic diaries and caregiver observers
  • Intelligent consent

The latest ecoa case studies

White Papers & Reports

A results-focused look at cardiometabolic trials at Medable

With GLP-1 therapies reshaping the competitive landscape, sponsors need speed to first patient, portfolio consistency, and adherence that holds up over years, not weeks. See how five sponsors/CROs got there with Medable.

White Papers & Reports

Medable oncology solutions

Discover how Medable’s AI-powered oncology platform simplifies complex cancer trials by integrating eCOA, ePRO, and eConsent solutions—reducing trial time, improving patient retention, and enhancing data quality for faster, more efficient research.

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White Papers & Reports

Accelerating oncology research: Digital strategies for modern clinical trials

Learn how digital tools ease oncology research for all stakeholders while accelerating the pace of research with this whitepaper.

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See how Medable can transform your trials.