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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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ebook

The Ultimate Guide to the EU MDR General Safety and Performance Requirements

(cover) Ultimate Guide to EU MDR GSPR

Download this Free eBook to receive the complete version of the guide covering the new General Safety and Performance Requirements (GSPRs), which must be implemented by medical device companies under the EU Medical Device Regulation (MDR 2017/745).

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