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.


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. 


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.

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.


500 +

MedTech Clinical Trials

Study Setup in 2-3


Support for 40 +

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