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There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Get help to classify textiles and which headings and codes to use.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
This guidance is for staff and managers working in adult social care settings (ASC). It gives information on multidrug-resistant organisms and principles on how to prevent the spread of these pathogens.
When and how to test for salmonella if you breed turkeys, and what happens if a flock tests positive. Testing is part of the salmonella national control programme (NCP).
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
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