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Data, Freedom of Information releases and corporate reports
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
This collection contains the Treasury's quarterly reports to Parliament, on its operation of the UK’s asset freezing regime.
How to get fast-track approval of medical devices during COVID-19.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Advice on writing clear notices and maximising replies to your FSNs.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
UK Health Security Agency (UKHSA) proficiency testing (PT) samples for food microbiology in freeze-dried format.
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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