Seamless, compliant, and timely study startup for sponsor and CRO study teams.

Build eCOA both validated instruments and eDiaries to industry standard.

Store instruments, including translations, in your library for rapid deployment that scales across future studies.

Dashboards and reports to stay up-to-date with all study and participant activity

Access and integrate a global library and marketplace of instruments, digital endpoints, and other trial tools. 

Make Data Collection a Breeze 

Make data collection a breeze with methods designed to fit into your participant’s everyday lives.

Remove manual entry and configuration with intuitive and automated workflows for sites and study teams.

Get the complete picture

Stay closer to your trial and make quicker, more informed decisions with expanded data sources and an aggregated view of the evidence being generated.

See your trial’s progress at a glance with easy-to-use dashboards and reporting.

Global expertise and compliance

Rest assured, our standardized, pre-validated builds have undergone scientific review to meet eCOA design best practices. Medable’s Patient-First Data Collection is FDA, CFR21 Part 11, HIPAA, and GDPR compliant.

Our eCOAs are designed, built, and implemented with user experience at the forefront - be that the participant, a clinician, a caregiver - and a strong emphasis on accessibility. They are built to adhere to industry best practices and undergo scientific review, so we can feel confident in the data we’re collecting with them.

Florence Mowlem, PhD.

Senior Director, eCOA Science & Solutions

Related articles

What Is eCOA? Improving Clinical Trial Data Quality
Read more
Connecting in new ways: Our partnership with Withings Health Solutions
Read more
Patient perspectives: a year of pharma webinars showcase what’s working and what needs work
Read more