Vigilance and adverse event reporting

This section sets out how the MHRA monitors the safety of devices and gives all the relevant information on reporting adverse incidents involving medical devices, including details on the updated online reporting system. It also provides the obligations on manufacturers for reporting adverse incidents and field safety corrective actions to the MHRA.


 

Adverse incidents - our role

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Reporting a non-compliant medical device (external link)

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Reporting adverse incidents involving medical devices

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Vigilance

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Page last modified: 06 January 2012