MDR/IVDR Training for Healthcare Professionals - Medical Device Regulation Course

MDR/IVDR Training

MDR/IVDR Training

Regulatory Compliance

Clinical Engineering in European Hospitals

Educational Content Only: This training is for informational purposes only. It is not an accredited or externally verified course and does not replace your facility's official policies or HPRA guidance.

Quick Actions

Frequently used tools and resources

Device Classification Wizard

MDR Annex VIII classification tool

Quick Reference Guide

Key articles, timelines & contacts

Practice Scenarios

Ward-level incident & recall exercises

Progress & Certificates

Track completion and download CPD certs

MDR/IVDR Training Programme

Self-paced training on EU Medical Devices Regulation (2017/745) and In Vitro Diagnostic Regulation (2017/746) for healthcare professionals in Irish and EU settings.

Content aligned with current HPRA guidance and MDCG documents.

Resources

Articles & Guides
Regulatory Glossary
Regulatory Library
FAQ

External References

HPRA — Medical Devices
EU Commission — Medical Devices

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© 2026 MDR/IVDR Training Programme. Content based on EU Regulations 2017/745 and 2017/746 and associated MDCG guidance.

Always consult your facility's clinical engineering department and the HPRA for site-specific guidance.