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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Document Management Training Management CAPA Management Audit Management Product Development

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Accelerate development with integrated design control and risk software.

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Design Controls Risk Management Risk Intelligence

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Data collection and management designed for MedTech clinical trials.

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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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Clinical Evaluation Procedure Template

Clinical Evaluation Procedure Template - Slide-in-covers

A free template to help you get started with creating your medical device company's clinical evaluation standard operating procedure (SOP) in accordance with EU MDR 2017/745.

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