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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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