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What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information and guidance on a range of medical devices for users and patients.
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.
Information about the EU Regulations and their implementation in Northern Ireland
Service providers or government departments installing networking technologies in government shared buildings, known as hub buildings.
Using retractable or foldable aerodynamic rear devices on heavy goods vehicles.
Sets out special provisions for Crown development for dealing with security-sensitive information in planning applications.
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