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.


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!

Comments are closed.