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How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
A randomized evaluation of an innovative technology-led initiative to provide customized computer-based supplementary instruction
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
To protect your design outside of the UK, you usually need to apply in each country you want protection in.
How to comply with the regulatory requirements for manufacturing custom-made medical devices.
Check a list of software developers who can provide Customs Declaration Service software.
Find what you or your business may need before you hire someone to act directly or indirectly on your behalf.
You may need an individual guarantee or a customs comprehensive guarantee to enter goods into a customs special procedure and defer duty.
Guidance for businesses who have unregistered Community designs.
Use this form to request a certified copy of a design.
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