This petition was submitted during the 2019-2024 parliament
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.
More details
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
Show on a map the geographical breakdown of signatures by constituency
10,000 signatures required to get a government response