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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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The Leading Toolbox for MedTech Clinical Data Collection

Let our experts show you how to:

  • Easily navigate Greenlight Guru Clinical's intuitive interface
  • Quickly create advanced studies and make mid-study changes with our best-in-class study builder, with no need for programming
  • Simplify regulation compliance with ready-to-use compliance templates
  • Ensure high response rates and excellent data quality

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

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.

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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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With Greenlight Guru Clinical, it is easy to set up and allows us to utilize those medical device features, making study configuration and data entry easy.
Alison Moran

Clinical Affairs Manager, Loop Medical

A very smart and comperhensive tool, Easy to implement and to be used for all stackholders who are involved in the study - sponsor, CRA, physicians and coordinators.
Ronit Shtrichman

Clinical Director, Pulsenmore

Are You Ready to Experience the Greenlight Guru Difference?

Achieve peace of mind knowing your EDC can stay ahead of compliance changes.

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500 +

Medtech clinical trials

study setup in 2-3

weeks

support for 40 +

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