# CLINICAL TRIAL SOLUTION Conduct more efficient & inclusive studies with an easy-to-use platform 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. ### 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. ### 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. ## Global Clinical Trial Compliance ## Contact us to learn more.