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.

$ インストール

git clone https://github.com/nimeshgurung/artifact-hub-collections /tmp/artifact-hub-collections && cp -r /tmp/artifact-hub-collections/skills/raw/alirezarezvani/claude-skills/ra-qm-team/mdr-745-specialist ~/.claude/skills/artifact-hub-collections

// tip: Run this command in your terminal to install the skill