Patient-Focused Clinical Data Collection

Empower and Engage Your Patients

Collect clinical outcome data via email/SMS and empower subjects to complete anytime, anywhere - on any device. Collect outcome data in-person, remotely, or with a combined approach.


1,000+ of the world's leading MedTech companies trust Greenlight Guru.

Better Patient Experience, Better Data

Empower your patients and get better data, higher engagement, and lower patient dropout rates. Greenlight Guru Clinical is designed to take the patient experience to the next level and ensure minimal friction. Allow patients to complete questionnaires using their own device (BYOD). There is no application to install, patients can easily and securely fill out forms directly in their browser of choice. 


The Ideal ePRO for Medical Devices

Developed for the perfect combination of easy setup, simple data compliance and
great user experience.

Simplify Study Management

Lean back and stop spending unnecessary time on managing reminders and study data. Automatic study flow, distribution of questionnaires and patient reminders on email or SMS make study management far less complex and time-consuming. 

Gain Complete Data Overview

Combine your ePRO data with clinical data collected via other sources such as eCRF or wearables - all stored in a single secure location with real-time data access. 

Ensure Traceability

Never worry about data traceability again! by Greenlight Guru Clincial's automatic subject identity validation ensures full traceability of all data inputs.

Enable BYOD

Build smart questionnaires that patients can complete using their own computer, laptop or mobile. There is no application to install, patients can easily and securely fill out forms in their preferred browser without downloading anything. 

Built to Make Data Collection Easier

Your unique device requirements are our standard.

See More of Our ePRO Software

Get a deep dive into our ePRO software and see how it can take your outcome data collection to the next level.


500 +

MedTech Clinical Trials

Study Setup in 2-3


Support for 40 +

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