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Change to the information provided on adverse events in the Summary of Product Characteristics (SPC).
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Vaccination newsletter for health professionals and immunisation practitioners.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Use the Agent Updates to get HMRC guidance if you're a tax agent or adviser.
News and information about updates for each inspection data summary report (IDSR) release, including any new functionality, features and bug fixes.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What you need to know about the Environment Agency’s new national risk information for flooding and coastal erosion.
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