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.

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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

The European Union (EU)'s MDR goes into effect May 2020.

Watch the Webinar

In this this webinar, you will learn:

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