Notified Bodies: Certifying Your Products Under the EU Medical Device Regulation

[Guide]Notified Bodies: Certifying Your Products Under the EU Medical
Device Regulation

Medical device companies must certify their products under the new European Union (EU) Medical Device Regulation (MDR) by May 2020. As the deadline approaches, many companies have yet to acquire the data they need to take to their notified bodies and get approved for the certification.

What’s Included in This Guide?

This guide explores the role of notified bodies, the process toward certifying products under the new EU MDR legislation, and a listing of organizations currently registered to provide the certification.

Key Insights Include:

New EU MDR requirements.
An overview of notified bodies.
Notified bodies’ data requirements.
A review of current notified bodies.
…And more!

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[Guide]Notified Bodies: Certifying Your Products Under the EU Medical Device Regulation

What’s Included in This Guide?

Key Insights Include:

[Guide]Notified Bodies: Certifying Your Products Under the EU Medical
Device Regulation