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UK Device Safety To Be Enhanced By Patient Safety Commissioner

 
• By Ashley Yeo

Certain Cumberlege Review recommendations are making their way into draft UK legislation as the government presses ahead in shaping the UK’s post-Brexit devices regulatory system.

Sharaf Maksumov

A new UK role of patient safety commissioner, providing independent oversight and guidance on patient safety elements relating to device and pharmaceutical product use and surveillance, has been proposed for inclusion in the Medicines and Medical Devices (MMD) bill. The bill is currently going through parliament.

This was one of the recommendations to emerge from the July 2020 report on the Independent Medicines and Medical Devices...

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More from Europe

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EU4Health Boost For Orphan Devices And SMEs

 
• By Ashley Yeo

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• By Ashley Yeo

In return for building a successful US export business, Switzerland has been handed a 39% tariff effective immediately by the Trump administration. Diplomatic channels have been reopened to undo the tariff. Meanwhile, the medtech industry is looking to develop OUS markets for Swiss exporters.