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The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
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.
Help available and steps you should take if you have a medical emergency or are hospitalised abroad, including for planned treatment.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
Information about support for British nationals experiencing mental health difficulties in The Netherlands.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
How to apply for an exceptional use authorisation to place medical devices on the UK market.
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