Clinical Login Support Contact Sales
Products

More than a Quality Management System: Tools for the entire MedTech Lifecycle.

Learn More

Featured Capabilities:

Document Management Training Management CAPA Management Audit Management Product Development

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

View Product Tour

Accelerate development with integrated design control and risk software.

Learn More

Featured Capabilities:

Design Controls Risk Management Risk Intelligence

Schedule a custom demo of Greenlight Guru Product now.

REQUEST A DEMO

Data collection and management designed for MedTech clinical trials.

Learn More

Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys Product Add-Ons

Get a personalized demo of Greenlight Guru Clinical today.

Request a Demo
Solutions
Why Us
Customers
Partners
Company
Resources
ROI Report Cover

Calculate Your ROI
Pricing
Request a Demo
Request a Demo

 

Pre-validated & GCP compliant surveys

The Ideal Post-Market Survey Tool for MedTech

Collect scientifically valid and compliant post-market data with Greenlight Guru Clinical’s market leading data collection tool, specifically built for medical device and diagnostics post-market surveys under EU MDR and FDA.

REQUEST A DEMO

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

Pre-Validated Post-Market Surveys

Don’t risk your device’s market position with flawed post-market data! Ensure optimal and compliant post-market survey data with minimum effort and resources. The Greenlight Guru Clinical Survey tool comes pre-validated per ISO 14155:2020 and enables GCP compliance out-of-the-box. All to help you set new standards for your post-market data quality. 

 REQUEST A DEMO

Get your Post-Market Surveys Right!

We’ve built the ideal post-market survey tool for your device, so you can focus on improving the quality of life for your patients.

Maintain Data Overview

Integrate your post-market survey data with the Greenlight Guru Clinical platform and manage all your data collection in one system.
Fast to Set up, Easy to Repeat

Set up your post-market survey easily with our intuitive study builder, and clone and repeat your surveys infinitely. 
Ensure Traceability


Never worry about data origin validation again! All data inputs automatically include automatic user identification to ensure full traceability from source to sponsor.
Simplify Clinical Data Compliance

Greenlight Guru Clinical Survey is pre-validated and compliant with ISO 14155:2020 requirements, enabling you to easily collect GCP compliant post-market surveillance data. Additionally, Survey simplifies compliance with MDR, FDA CFR 21 Part 11, GDPR, and more.

Post-Market Surveys Shouldn’t Be Hard

Designed to streamline your entire post-market clinical data collection process, minimizing time and resources needed to ensure consistent, high quality data.

Easy Study Setup

Fast and intuitive 3-step study builder. Create any study within 90 seconds.

Send Survey via Email, SMS, or QR-Code

Versatile survey distribution to ensure high patient engagement.

White Labeled User Interface

Enhance subject experience by using your own logo and name for all subject communication.

Automatic Subject Validation

Enjoy automatic SMS validation of subject identity to ensure full data traceability.

REQUEST A DEMO

 

 
https://blog.greenlight.guru/hubfs/White%20label%20jpg.png
https://blog.greenlight.guru/hubfs/authentic%20%20phone-1.png

See More of Our Survey Software

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

REQUEST A DEMO

500 +

MedTech Clinical Trials

Study Setup in 2-3

Weeks

Support for 40 +

Languages
Search Results for:
    Load More Results