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.