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

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Featured Capabilities:

Document Management Training Management Product Development Design Control Risk Management CAPA Management Audit Management

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

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Data collection and management designed for MedTech clinical trials.

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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

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Ultimate Guide to Comparing Quality Management System Solutions

This eBook compares the best QMS software solutions to help medical device companies make an informed decision when investing in a quality management system.

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Greenlight Guru for Clinical
Data Managers

Collect high-quality, compliant data from clinicians, patients, and any other users—and manage it all in the same system. Built specifically for MedTech, Greenlight Guru is the only clinical data solution you’ll need, from premarket studies to post-market surveillance and PMCF activities.

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All your clinical data, all in one place

Whether you're preparing for a pilot study or sending out post-market surveys, Greenlight Guru makes it easy to collect and manage all your clinical data in a modern, compliant, and user-friendly system. Say goodbye to paper and hello to intuitive design and unrivaled visibility into your data.

Why Clinical Data Managers Love Greenlight Guru

Endless data capture options

With a full suite of eCRF, ePRO, post-market surveys, and ad hoc data collection methods, you never miss out on crucial clinical data.

Mobile-friendly and modern collection options mean higher response rates, better adherence, and excellent data quality.

Compliant and prevalidated

Greenlight Guru’s EDC system comes pre-validated per FDA, EU, and ISO 14155:2020 requirements, so you can begin your clinical activities in compliance and stay that way.

Ready-to-use and customizable compliance templates, combined with in-house industry experts, mean you’re never on your own.

User-friendly

Our no-code solution ensures that anyone can quickly learn how to use Greenlight Guru, create studies, and navigate the system with ease.

Build studies in as little as 90 seconds, reuse forms and studies to save time, and get real-time insight into your data.

Made for MedTech

An EDC for medical device, IVD, and SaMD clinical trials.

MedTech studies are different. That’s why you won’t find expensive, pharma-centric features in Greenlight Guru’s EDC system.

You’ll have everything you need to collect and manage high-quality clinical data—and nothing you don’t.



1,100+ of the world’s leading MedTech companies trust Greenlight Guru.

“Our partnership with Greenlight Guru has meaningfully influenced our success by directly impacting operations efficiency and adherence to timelines.”
Lucie Pribylova
Commercial Operations, HEMEX
“Data monitoring is much easier now than it was before. It's much easier to follow the participant flow and see the status of each participant. Before, we had to write to the site and ask for that status.”
Sarah Nygaard Jensen
Clinical Project Manager, InnoCon Medical
“Having everything-informed consent, randomization, and the eCRFs and ePROs- all in one system makes it much easier to finish the study on time. The teams at our study sites also really value that they don't have to work with more than one system.”
Heiða Bragadóttir
Clinical Trial Manager, Sidekick Health
“The requirements for medical devices are very different from the requirements of pharmaceutical trials, so we needed and EDC solution specifically for medical devices.”
Martijn Dekkers
Clinical Research Manager, Medartis

The best medical devices start with the best clinical evidence.

It all starts with the right tools.

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500 +

MEDTECH CLINICAL TRIALS

study setup in 2-3

weeks

support for 40 +

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