Real-World Evidence (RWE) Solution

Greenlight’s cloud-based, unified, configurable, flexible solution is purpose-built to achieve real-world research goals

- - Efficiently compile meaningful data to establish evidence of clinical, economic, and humanistic (patient-centric) value in actual practice settings
  - Support safety event tracking and adjudication under actual practice conditions
  - Minimize participant data collection burden while maximizing participant engagement (at all study stages)
  - Appropriately access and utilize available RWD to augment prospective data collection
  - Support the needs of Medical Affairs / RWE / HEOR teams in conducting relevant and informative real-world research, and in communicating findings
    
    Greenlight powers RWE studies of all varieties, including:
  - Site-based observational studies
  - Direct-to-patient studies
  - Patient registries (disease, product)
  - Post-approval safety surveillance
  - Burden of illness studies
  - Long-term extension / follow-up studies

Prototype in as little as 48 hours.

Adopted by 350+ research sites.

Serving 800K+ end users.

More Smart Technology.
Less Costly Services.

Greenlight’s easy-to-use clinical trial solution is available in self-serve and managed service models. We combine our expertise and technology to deliver a unique solution, including:

✔ Rapid study setup using no-code tools.

✔ Library of integrated devices and industry services.

✔ Flexible implementation options.

✔ Automated workflows reduce study team burden.

✔ User experience patients and study teams love.

A Better Way to Manage RWE Studies

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

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

Reduce patient burden and boost retention with engaging experiences

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.