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EU Industry Tells Authorities To Get Their Act Together As Pressure Builds

 
• By Amanda Maxwell

Six months into the transition period for the EU's Medical Device and IVD Regulations, the structures and resources needed to help medtech companies comply with the new rules are still far from being in place. Industry association MedTech Europe's concerns are mounting.

MedTech Europe, the EU's largest association representing medical device and IVD manufacturers, has issued several position papers calling for swift action from national and EU authorities to implement the new Medical Device and IVD Regulations (MDR and IVDR) within the foreseen timeframes.

Their appeal to the authorities to ensure the necessary foundations are in place comes less than two weeks after the publication of the EU's long-awaited roadmap to the implementation of...

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