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UK MHRA Plans Revised Device Roadmap By End Of 2024

Agency Seeks Pragmatic Approach To IVD Regulation

 
• By Ashley Yeo

The milestones on MHRA’s in-progress medtech regulatory roadmap for Great Britain will be subject to some change in the coming months.

Stethoscope with national flag conceptual series - United Kingdom

The UK Medicines and Healthcare Product Regulatory Agency (MHRA) has released new outline dates for elements of the Great Britain medtech regulatory roadmap, which was published in January.

Laura Squire, the agency’s chief quality and access officer, wrote in a recent MHRA official blog that work on revising...

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FDA Changes Fail To Diminish US Appeal To European Medtech Industry

 
• By Amanda Maxwell

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EU4Health Boost For Orphan Devices And SMEs

 
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More from Policy & Regulation

Brazil’s Medtechs Look To Solutions After 50% US Tariff Hit Amid ‘Scenario Of Uncertainty’

 
• By Bernard Murphy

Hopes that last-minute negotiations might exempt Brazil’s $300m medtech exports from the latest round of US tariffs have been dashed, leaving the industry braced for further market instability that countermeasures could trigger.

Survey Reveals Gaps In Medtech Compliance Processes

 
• By Elizabeth Orr

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Environmental Group Questions FDA’s Stance On PFAS In Medical Devices

 
• By Brian Bossetta

The US FDA says PFAS used in medical devices are safe and that there’s no reason to restrict them in device production. An environmental group finds the agency’s assertion questionable.