Petition Commission an independent safety audit of MHRA on medicine & device approval

Commission an independent safety audit of MHRA into their process for approving medicines, medical devices & ongoing surveillance.

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Processes should be benchmarked against other regulators, including CAA & ONR.

Auditors must be from outside of the pharmaceutical industry & have no industry links.

A wide range of medicines & devices have caused patient harm. These have been approved by MHRA. It has often taken years to react to safety signals e.g. mesh, Primodos & Valproate.

We believe the MHRA is focusing too much on clinical trials of new medicines, rather than safety of existing ones.

There is a 'revolving door' between industry & the regulator, several board members declare conflicts of interest.

MHRA is primarily funded by the pharmaceutical industry.

This petition is closed This petition ran for 6 months

3,533 signatures

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Date closed 23 November 2023
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