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Submitting Adverse Incidents with Medical Devices to the MHRA

Submitting Adverse Incidents with Medical Devices to the MHRA

The NHS Implant Analysis Service is delighted to see the announced changes and improvements being implemented by the MHRA regarding adverse incident reporting for medical devices. These are significant quality-of-life changes that remove some of the friction from reporting. Anything that can be done to encourage robust reporting of all potential incidents is to be welcomed, as this is the only way these incidents can be appropriately investigated and any issues identified and remedied to improve patient safety.

For full details of the improvements, please see the full article below:

Submitting Adverse Incidents to Medical Devices to the MHRA – enhancements to the MORE portal – BIVDA Newsletter

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