Clinical Trial Solution

Greenlight delivers something rare in our industry—easy-to-use technology and happy customers. Our unified platform offers no-code tools, configurable automation rules, robust clinical trial features, and user experiences study teams and patients love, available in self-serve and manage-service models.

Greenlight’s platform is trusted by life science, CRO, and academic customers to conduct studies of all kinds, from single-site research to global phase III trials, including support for hybrid and decentralized clinical trials (DCT). Our purpose-built platform makes it easy to create engaging patient experiences that improve trial participation and efficiency while reducing burden for everyone involved.

Prototype in as little as 48 hours.

800K+ end users, 350+ sites.

Loved by patients and sites.

More Smart Technology.
Less Costly Services.

✔ Rapid study setup using no-code tools.

✔ Library of integrated devices and industry services.

✔ Automated workflows reduce study team burden.

✔ User experience patients and study teams love.

✔ Self-serve and managed service models.

A Better Way to Manage Clinical Trials

Greenlight supports trial designs of all varieties, from site-based to hybrid and fully decentralized. Our unified platform is built to power studies from end to end and can interoperate with any existing eConsent, eCOA, EDC, and EHR vendors.

Implement Protocol Design
No-code Configuration
eCOA Library
Activity Library

Screening
Health Record Access
eConsent
Enrollment
Education
Telehealth Screening
Randomization

Connected Devices
eCOA
Engagement
Televisit
Educational materials
Activity tracking
Notifications & Reminders
Communication
Medication Adherence

Automated Workflows
Site & Study Team Apps
APIs
Real-Time Analytics
Cloud Infrastructure

PARTICIPANT EXPERIENCE

Engaging experiences reduce burden while boosting retention and adherence.

Eligibility Screening

Access broader populations & identify suitable participants. Deploy pre-screening questionnaires to filter inclusion/exclusion criteria.

eConsent

Seamlessly obtain informed consent. Our electronic records and signatures are 21 CFR Part 11 compliant.

Communication

Engage with participants 1:1 and in groups through in-app messaging as well as email and text.

Onboarding

Introduce participants to your study and app. Improve retention and engagement through early education.

eCOAs & ePROs

Use surveys to collect patient outcome data. 100+ commonly-used COAs & PROs pre-built.

Connected Devices

Capture biometric data from devices, sensors, and wearables. Existing integration and flexibility to support your preferences.

Educational Content

Engage and inform participants with information about your study over text and video.

Adherence Framework

Personalize and engage at scale using an automated, data-driven approach. Customize experiences based on eCOA results, biometric data, and more.