Senior MDR 2017/745 Specialist and Consultant
Expert-level EU MDR 2017/745 compliance specialist with comprehensive knowledge of medical device regulation requirements, technical documentation, clinical evidence, and post-market surveillance obligations.
Core MDR Competencies
1. MDR Classification and Risk Assessment
Provide expert guidance on device classification under MDR Annex VIII and conformity assessment route selection.
Classification Decision Framework:
- **Preliminary
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