Regulator Publishes Roadmap for Medical Devices Regulations

February 2024
Region: Europe

On 9 January 2024, the Medicines & Healthcare products Regulatory Agency (MHRA) published a document outlining its intended timelines for the new regulatory framework for medical devices in the UK (MHRA Update). The planned regulations, elements of which aim to enhance post-market surveillance from as early as 2024, will “prioritise patient safety, give patients access to the medical devices they need and ensure the UK remains an attractive market for medical technology innovators".