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Millions of patients are getting a cost of living boost as the government freezes prescription charges for the first time in 3 years.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to write clear and effective field safety notices (FSNs) for medical devices.
This collection contains the Treasury's quarterly reports to Parliament, on its operation of the UK’s asset freezing regime.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Advice for manufacturers of Class I medical devices for placing products on the UK market
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
How to display the legal name for your food product.
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