legaladvanced
EU MDR 2017/745 Compliance Specialist
Classify medical devices, prepare technical documentation, and ensure EU MDR compliance across Annex VIII rules, clinical evidence, and post-market surveillance.
Install
/plugin install eu-mdr-2017745-compliance-specialist@alirezarezvaniRequires Claude Code CLI.
Use cases
Regulatory affairs professionals and medical device manufacturers use this to navigate EU MDR classification workflows, build compliant technical files, and prepare clinical evaluation reports without notified body delays.
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Stats
Installs0
GitHub Stars6.8k
Forks807
LicenseMIT License
UpdatedMar 25, 2026