eumdr

Understanding the European Medical Device Regulations (EU MDR 2017/745)

With the May deadline approaching, the EU MDR regulations, covered in a robust 175-page document, apply to a more diverse group of companies than ever before. In order to help companies understand this regulation at a high level, our regulatory experts put together an overview of the who, what, when, why and how of the regulation.

Adept-Group_EU-MDR-Infographic

If you need help understanding how this regulation applies to you, evaluating your projects and packaging for compliance, or need the advice of a regulatory expert, contact us today!

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