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

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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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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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What Influences SaMD Classification?

If you’re developing a SaMD (Software as a Medical Device), then the product classification will impact what is required of you in terms of paperwork. It’s important to understand your classification in terms of risk. Learn the important factors of SaMD classification.

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Featured Capabilities:

What Influences SaMD Classification?

What Influences SaMD Classification?

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