UK MHRA In The Spotlight As Cumberlege Review Puts Medtech Safety At The Top Of Health Agenda

The findings of the Cumberlege Review into how safety issues for three medical product groups were handled will shape debate on the UK’s new devices legislation, now going through parliament. The MHRA’s devices regulatory activity also comes in for scrutiny.

Patient safety

The Baroness Cumberlege Review of long-standing UK patient safety concerns relating to three groups of medical products, entitled First Do No Harm ̶ The report of the Independent Medicines and Medical Devices Safety Review, was published on 8 July.

Delayed as a result of COVID-19, the review, commissioned in 2018, recommends how the health care system in England can act faster on reports of harmful side effects from drugs...

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