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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
How to conform with the legal requirements for placing medical devices on the market.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
If your organisation supports people in Copeland, Allerdale or Warrington you may be eligible to apply for a grant/reusable equipment.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
This document outlines guidance for cleaning and decontamination of non-healthcare settings.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Information about how the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
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