Medical Device Masterclass

Watch the Masterclass

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This new EU MDR regulation is complex, presenting a data and design dilemma for Medical Devices companies, as product labeling will undergo greater scrutiny in the name of patient safety.

Key Learning Objectives:

  • Best practices to improve your artwork and labeling process, while achieving compliance and reducing risk of recalls.
  • How you can successfully track label changes, manage your packaging content process, and meet the MDR deadline.
  • How structured content management can drive efficiency in your end-to-end process.
  • Demonstrations of labeling and artwork management and content control.