MDR 2017/745 - CONSULTING

MDR 2017/745 - CONSULTING

Consultancy, Reports, Analysis

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Our MDR Consulting Services ensure full compliance with European regulations MDR 2017/745 for medical devices. The MDR is a law that regulates the manufacture, sale and use of medical devices across the European Union (EU). It was passed in 2017 and became applicable in 2021. It aims to protect the health and safety of patients by ensuring that medical devices are safe and effective.

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