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This petition was submitted during the 2019 to 2024 Parliament

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

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

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.

3,533 signatures


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    If this petition gets 10,000 signatures, government will respond to it.

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    This petition will stay open until 23 November 2023.