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How to conform with the legal requirements for placing medical devices on the market.
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This section of the SEPs Resource Hub signposts to international SEPs-specific information, including for the purposes of patent applications.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
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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.
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