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Government to align with European specifications on high risk in vitro diagnostic devices to reduce regulatory burden

News Healthcare & Pharma Law & Policy Updates
Date: 10th Jul, 2025 Source: Medicines and Healthcare products Regulatory Agency (MHRA) Country: United Kingdom Original Source

Brief

On August 10, 2025, the Medicines and Healthcare products Regulatory Agency (MHRA) issued an update regarding Government to align with European specifications on high risk in vitro diagnostic devices to reduce regulatory burden. The move aims to enhance patient safety by introducing new performance standards for IVD devices related to infectious diseases.

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Medicines and Healthcare products Regulatory Agency (MHRA)

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