The European Union (EU)'s MDR goes into effect 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.

Watch the Webinar

(*) Required field
By using Esko's services or submitting your details, you agree to our Privacy Policy.

In this this webinar, you will learn:

  • What information and symbols are required on your medical device labels to comply with MDR
  • Best practices to improve your packaging 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
Esko
Contact us


Subscribe