Clinical Electronic Data Capture (EDC) Software

The Leading Toolbox for MedTech Clinical Data Collection

Collect clinical evidence, safety, and performance data for any activity, throughout your entire medical device lifecycle. All within one compliant platform.

MedTech Clinical Solutions

Every Feature Made for MedTech

Your software is already optimized for medical device studies. That means no coding, no stressful setup, and no expensive pharma-centric features you'll never use.

Pre-validated per FDA and ISO 14155:2020

Ensure compliance from the start with built-in ISO 14155:2020, EU MDR, and FDA requirements. In addition, you'll get 13 ready-to-use and customizable compliance document templates.

Support for multi-indication device studies

Easily make adjustments to your study designs according to different countries' requirements and EC approvals.

Support for dynamic visits and treatments

If your study subjects require one or many treatments with your device, you can use multiple activations for any visit event.

3-Step study builder

Set up a study in as little as 90 seconds with intuitive drag-and-drop elements, form validation, and customizable protocol designs. Adjust and reuse your studies as much as you need to.

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Platform Tools

Functionality Meets Convenience

Experience versatile tools and customizations that anyone can use and build your study exactly as you need it.

eCRF: Customizable case report forms


Design your eCRF based on your unique study requirements — simple or complex, there are no limits.

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ePRO/eCOA: Secure SMS and Email data collection


Create a user-friendly experience for study subjects and increase response rates, adherence, and quality of data.

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Survey: Pre-validated post-market surveys


Out-of-the-box GCP-compliant surveys. Collect data with dynamic surveys to comply with EU MDR PMCF or FDA Post-Approval requirements.

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Cases: GCP compliant ad hoc data collection


The mobile-first case studies series data collection tool you've always wanted. Clinician-friendly and compliant. Enable ad-hoc data entry of high-quality patient data in post-market settings.

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Add-ons: Build your study toolbox

From eConsent to randomization, custom study dashboards, and external system integrations.

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

When we teach people to use it, they just fly through it, even when they're not used to using systems like this.
Ragna Björg
Sr Director of Product Management at Kerecis
It is now super easy and flexible for us to create each page of our eCRF.
Barbara Simon
Clinical Research Audiologist at Bernafon
The API connection with our own software saves an incredible amount of internal resources.
Audrey Plesse
Clinical Project Manager at Cardiologs
We've managed to cut weeks of work out of our clinical tests.
Karen Boel
Head of Clinical Audiology and Usability, SIV at Oticon

Watch Us Build a Clinical Study in 90 Seconds:

We'll show you how.


Better Clinical Evidence.
Safer Medical Devices.

It starts with the right tools.


500 +

MedTech Clinical Trials

Study Setup In 2-3


Support for 40 +

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