Introducing our comprehensive and invaluable resource for navigating the complexities of medical device regulation in the European Union, the Practical Guide to the EU Medical Device Regulation (EU) 2017/745. Written by industry experts with extensive experience in the day-to-day interpretation and application of the MDR, this guide provides clear and concise answers to practical questions that arise in the development, manufacturing, and marketing of medical devices.
Our guide also contains the latest legislative changes, including the amending Regulation 2023/607, ensuring that you are up-to-date with the most current regulations and requirements. Whether you are a medical device manufacturer, importer, distributor, or other stakeholder, this guide will be an invaluable tool in ensuring compliance and success in the EU market.
Practical Guide to the EU Medical Device Regulation
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