Is Your Product Packaging MDR Compliant?
The European Union (EU)'s MDR goes into effect on May 2020. This new regulation is complex, presenting a data and design dilemma for Life Science companies, as product labeling will undergo greater scrutiny in the name of patient safety.
Are you prepared to meet those label changes?
In this webinar, you will learn:
• What information and symbols required on your medical device labels to comply with MDR
• What are the best practices to improve your end to end packaging and labeling process from design brief to print, while achieving compliance and reducing risk of recalls
• How you can simplify your packaging content management process to operate and track the label changes and successfully navigate through the MDR complexity and meet the deadline