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.

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.

STUDY MANAGEMENT

Easy-to-use tools for study teams, sites, and providers.

Onboarding & Randomization

Deploy effective onboarding programming and randomize participants into study groups.

Data & Analytics

View dashboards and reports in the console, export to CSV, or access via API. Look at historical, real-time, and forecast data.

Participant Monitoring & Engagement

Monitor biometrics, view historical and real-time data, modify care plans, send automated or manual messages, and more.

Workflow Automation

Automate tasks and workflow to improve clinical process. Our rules engine is flexible, easily- configurable, and powerful.

Permissions Layers

Permission controls provide the proper level of access and features to each user, from data manager to study leadership.

Global Clinical Trial Compliance

Contact us to learn more.

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