# REAL-WORLD EVIDENCE SOLUTION

Evidence and engagement : The new gold-standard for real-world research

### 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

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## **Prototype in as little as 48 hours.**

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## Adopted by 350+ research sites.

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## **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.

### 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.

## Secure & Compliant

## Contact us to learn more.