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.
85
70%
Does it follow best practices?
Impact
96%
0.98xAverage score across 6 eval scenarios
Passed
No known issues
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