Software Development
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.
- Publisher / source
- davila7/claude-code-templates (found on skills.sh)
- Upstream record
- davila7/claude-code-templates
- Version
- Version 2
- Published
- Publication review
- Approved for publication
- Content fingerprint
f335e8753538a6fdc8273b0dedd5381d07fb2fcd69deca298ab08604a7cf6ae7