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mdr-745-specialist
EU MDR 2017/745 regulation specialist and consultant for medical device requirement management. Provides comprehensive MDR compliance expertise, gap analysis, technical documentation guidance, clinical evidence requirements, and post-market surveillance implementation. Use for MDR compliance assessment, classification decisions, technical file preparation, and regulatory requirement interpretation.
#compliance#legal#medical-device#regulatory
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Repositorydavila7/claude-code-templates
Stars22,267
Last UpdatedMar 7, 2026
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