Mdr 745 Specialist

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

作者 alirezarezvani19392f7a0826無授權條款27K 個星標收錄於 2026年10月8日更新於 2026年10月8日儲存庫5 週前更新

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').

包含腳本Business & Finance

僅公開檔案列表。將技能安裝到工作區後即可檢視檔案內容。

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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

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來源:alirezarezvani/claude-skills位於ra-qm-team/skills/mdr-745-specialist提交19392f7

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