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MDR/IVDR Training
Regulatory Compliance

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Find specific information across all training modules, rules, FAQ, and resources

Popular Searches

Common topics searched by healthcare professionals

Device classification
Incident reporting
Class III devices
IVDR compliance
UDI requirements
Post-market surveillance
CE marking
Clinical evaluation
Risk management
Notified bodies

Training Modules

Interactive learning modules

6 modules

Classification Rules

22 classification rules

22 rules

FAQ

Common questions answered

25+ questions

Resources

Downloadable guides

10+ downloads

Search Tips

Use specific terms:

  • • "Class III" instead of "high risk"
  • • "IVDR" for diagnostic devices
  • • "UDI" for device identification

Content types:

  • • Training modules for learning
  • • Rules for classification help
  • • FAQ for quick answers
  • • Resources for downloads