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Nipro April 2026
Volume 16 Issue 1

Fighting Counterfeits in the Medical Devices Sector –A Step Beyond the EU MDR

The counterfeiting of health products is a serious and growing concern, and it has come at the forefront of the public mind in recent years with several strict regul...
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News

MEDEI Issues MedTech Advisory on Mandatory EU Medical Device Regulation

MedTech data management enabler MEDEI ApS today released an Industry Advisory outlining changes and advice that medical device manufacturers can use to comply with t...
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PCI Launches High Containment Packaging Facility at Ireland Site, EU

Most recent EU acquisition and PCI’s latest site to offer state-of-the-art contained packaging facility to global customers for potent compounds Today, lead...
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Focus should be on public health and patient safety after EMA relocation decision, says Brexit Health Alliance

Responding to the announcement about the new location of the European Medicines Agency (EMA), Niall Dickson, co-chair of the Brexit Health Alliance, said: “The ...
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