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How to conform with the legal requirements for placing medical devices on the market.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
SIA regulation: how the SIA enforces the law and what the penalties are for breaking it.
Annexes of the Free Trade Agreement (FTA) between the United Kingdom of Great Britain and Northern Ireland and Australia.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Annexes of the Free Trade Agreement (FTA) between the United Kingdom of Great Britain and Northern Ireland and New Zealand.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
Product Safety Report for Govek KN95 Face Masks presenting a health risk.
Check which reservations are relevant to UK businesses selling services to customers in EU member states.
Guidance for manufacturers, importers and distributors.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Astronauts from the United Kingdom could fly to space on a future Axiom Space mission, thanks to a new agreement signed between the UK Space Agency and the Houston-based space company.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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