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What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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 MHRA for the markets in Great Britain and Northern Ireland.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
Information about the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
Using retractable or foldable aerodynamic rear devices on heavy goods vehicles.
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