Mdr 745 Specialist

alirezarezvani/claude-skills/ra-qm-team/skills/mdr-745-specialist

作者 alirezarezvani19392f7a0826无许可证27K 个星标收录于 2026年10月8日更新于 2026年10月8日仓库5周前更新

EU MDR 2017/745 compliance specialist for medical device classification, technical documentation, clinical evidence, and post-market surveillance. Covers Annex VIII classification rules, Annex II/III technical files, Annex XIV clinical evaluation, Art. 86 PSUR schedules, and EUDAMED integration. Use when classifying a medical device under MDR, building or gap-checking a technical file, planning clinical evaluation or PMS/PSUR cadence, or preparing for notified body review (e.g., 'what class is my device under MDR', 'review my PSUR schedule').

包含脚本Business & Finance

仅公开文件列表。将技能安装到工作区后即可查看文件内容。

路径大小类型
references/clinical-evidence-requirements.md9.2 KBtext/markdown
references/mdr-classification-guide.md8.7 KBtext/markdown
references/technical-documentation-templates.md10.1 KBtext/markdown
scripts/mdr_gap_analyzer.py17.7 KBtext/plain
SKILL.md10.2 KBtext/markdown

来源与署名

来源:alirezarezvani/claude-skills位于ra-qm-team/skills/mdr-745-specialist提交19392f7

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