Are you aware of EU MDR/IVDR deadlines? Explanations include a few surprises

The implementation timing of the EU’s new Medical Device and IVD Regulations is complicated. The texts expect the possibility of not having enough time to establish all the required structures, and, consequently, they include some intricate transitional arrangements. But many in industry have condemned the approach for being too difficult to understand.

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Posted on 18. Juni 2018
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