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Commission Predicts 43 Notified Bodies Under MDR And 12 Under IVDR By End November

 
• By Amanda Maxwell

Altered compliance timelines under the EU’s Medical Device and IVD Regulations give the sectors more time. But urgency remains for manufacturers to hire notified bodies to assess their products. Expanded capacity bandwidth is promised soon.

Business growth (ImageFlow/Shutterstock.com)
Number Of MDR And IVDR Notified Bodies Steadily Growing

By the end of this November, three more notified bodies should be officially designated in the EU under the scope of the Medical Device Regulation and one more under the scope of the IVD Regulation.

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Trump’s Preliminary 2026 HHS Budget Plan Protects US FDA User Fee Collection

 
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Looking Back Towards The Future

 
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