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How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
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.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
How to conform with the legal requirements for placing medical devices on the market.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How manufacturers or distributors of Coronavirus (COVID-19) test devices can apply for approval of their tests to be placed on the UK market.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
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