The European Medical Device Regulation
About the Book
The European Medical Device Regulations guidebook provides practical guidance on the implementation of the EU Medical Device Regulation (MDR). Originally published in 2020, it serves as the foundational resource for understanding regulatory requirements and expectations under the MDR framework.
To ensure customers receive the most current information, this guidebook is bundled with a 2021 e-book supplement that summarizes key regulatory developments and changes since the original publication.
The guidebook and supplement are intended to be used together.
Purchasing Options
This book can ONLY be purchased as part of the following bundles:
- Digital Guidebook + e-book supplement. Single purchase of the original guidebook and supplement; accessible online via RAPS Library online reader and downloadable.
- Printed Guidebook + e-book supplement. Single purchase of the printed guidebook; includes the electronic ebook supplement accessible online via RAPS Library online reader and downloadable.
