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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

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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

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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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checklists and templates

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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