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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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Periodic Safety Update Report Template

Periodic Safety Update Report Template - slide in cover (1)

A free resource to help you document all necessary components that must be included in your Periodic Safety Update Report (PSUR) in accordance with the requirements of EU MDR.

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

 

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