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MDR has been a hot topic in regulatory, PV, and, clinical circles for quite some time. We have led the way in writing and reporting about how MDR will impact the manufacturers, distributors, EU Authorised Representatives, and other specialists within the devices sector. We have compiled 10 expert-written articles from our dedicated medical devices team.
The MDR collection has 10 articles on issues such as:
- What will the impact be on economic operators?
- How will the role of the EU Authorised Representative change?
- What are the most important changes to be introduced in the new medical device regulations?
- What do you need to know about Clinical Evaluation Reports in MDR?
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