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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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BestQMS-book-mockup-01

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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checklists and templates

eIFU Requirements in the EU Checklist

eIFU Requirements in the EU - Slide-in-cover

Use this checklist to determine whether you meet a set of conditions, outlined in REGULATION (EU) 2021/2226, which allows certain device manufacturers (refer to Article 3) to provide electronic instructions for use (eIFU) to users, instead of in paper form.

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