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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 CAPA Management Audit Management Product Development

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

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Accelerate development with integrated design control and risk software.

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Featured Capabilities:

Design Controls Risk Management Risk Intelligence

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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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checklists and templates

Checklist: Design Transfer to Manufacturing

Checklist_ Design Transfer to Manufacturing - slide in cover

A free checklist you can use to confirm the development and approval of your design transfer activities, which will be used to compile your Device Master Record.

Want more free medical device resources? Click here to access our full library of downloadable content!

 

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© 2024 Greenlight Guru. All rights reserved. Legal Info