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Demystifying the Responsibilities of an EU Authorized Representative

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Discover the essential role of the European Authorized Representative (EU AR) for medical devices in Lorit Consultancy comprehensive guide

Verena Wieser talks about the pivotal responsibilities, from regulatory compliance to post-market surveillance.
Gain insights into how they support non-EU manufacturers navigate the complexities of EU regulations every step of the way.

Read more here.

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