MDCG Working Groups – EAAR Participation
- Stakeholder meeting
- Annex XVI
- Borderline & Classification
- Clinical Investigation and Evaluation
- Eudamed
- International Matters
- In Vitro Diagnostic Medical Devices
- New technologies
- Nomenclature
- Post-market Surveillance and Vigilance
- Standards
- UDI (Unique Device Identification and Device Traceability)