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mdr-745-specialist

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EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, and EUDAMED integration.

When to use

• medical device classification
• technical documentation
• clinical evaluation
• post-market surveillance
• EUDAMED integration
• UDI
• notified body
• PMCF

Skill page

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