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Greenlight Guru QMS

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

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Featured Capabilities:

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

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

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SMART-TRIAL by
Greenlight Guru

Data gathering and management designed for MedTech clinical trials and operations.

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Featured Capabilities:

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

Get a personalized demo of SMART-TRIAL by Greenlight Guru today.

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Greenlight Guru Academy

Learn valuable, career-boosting skills for the Medical Device industry. Get access to hundreds of free resources as well as subscription-based courses and certifications.

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Discover the new trends, outlooks, challenges, and opportunities in the MedTech industry in 2023.

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checklists and templates

15-in-1 MedTech Templates to Streamline Your Workflow

15-in1 Template Bundle

Are you looking to create new MedTech documents but not sure how to get started? You can save time with this 15-in-1 template bundle.

These templates are tailored specifically for MedTech companies and can help you quickly create documents for: Change Orders, FDA 483 warning letter responses, Training matrices, eCRF Forms, CAPA Reports, Risk management plan forms, Nonconformance reports, and more.

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