Loading...
Loading...
12 production-ready regulatory affairs and quality management skills for HealthTech/MedTech: ISO 13485 QMS, MDR 2017/745, FDA 510(k)/PMA, ISO 27001 ISMS, GDPR/DSGVO compliance, risk management (ISO 14971), CAPA, document control, and internal auditing. Python tools included (all stdlib-only). Works with Claude Code, Codex CLI, and OpenClaw.
npx skill4agent add alirezarezvani/claude-skills ra-qm-skills/read ra-qm-team/regulatory-affairs-head/SKILL.mdnpx agent-skills-cli add alirezarezvani/claude-skills/ra-qm-team| Skill | Folder | Focus |
|---|---|---|
| Regulatory Affairs Head | | FDA/MDR strategy, submissions |
| Quality Manager (QMR) | | QMS governance, management review |
| Quality Manager (ISO 13485) | | QMS implementation, doc control |
| Risk Management Specialist | | ISO 14971, FMEA, risk files |
| CAPA Officer | | Root cause analysis, corrective actions |
| Quality Documentation Manager | | Document control, 21 CFR Part 11 |
| QMS Audit Expert | | ISO 13485 internal audits |
| ISMS Audit Expert | | ISO 27001 security audits |
| Information Security Manager | | ISMS implementation |
| MDR 745 Specialist | | EU MDR classification, CE marking |
| FDA Consultant | | 510(k), PMA, QSR compliance |
| GDPR/DSGVO Expert | | Privacy compliance, DPIA |
python3 risk-management-specialist/scripts/risk_matrix_calculator.py --help
python3 gdpr-dsgvo-expert/scripts/gdpr_compliance_checker.py --help