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UK Shares How Its Medtech Regs Already Diverge From The EU: COVID-19 Marks The Start

 
• By Amanda Maxwell

The MHRA has updated its guidance on regulatory flexibilities for medical devices and medicinal products resulting from COVID-19 to highlight how its approach differs from the EU.

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While the UK Medicines and Medical Devices (MDD) bill continues through the government’s chambers and the future medtech regulatory relationship between the UK and the EU remains unknown, there is much speculation over the degree to which the UK is going to diverge from the EU when it comes to future medtech and pharma regulations.

Already, the Medicines and Healthcare products Regulatory Agency (MHRA) is taking steps to highlight where it has already taken adopted its own regulatory decisions; it has just updated its guidance...

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