Medical Innovation Exchange

Great Britain

UK Releases Draft Post Market Surveillance Requirements for Medical Devices

UK Releases Draft Post Market Surveillance Requirements for Medical Devices     The UK has released a draft of its proposed Post Market Surveillance Requirements for Medical Devices. If the draft regulations, “The Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2023,” are approved, they will pertain to devices sold in England, Wales, Scotland and …

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Bringing your Medical Device to the UK: What You Need to Know about UKRP

Bringing your Medical Device to the UK: What You Need to Know about UKRP     When it comes to medical device regulations, it is a time of transition for a number of countries. Both the EU and the UK are in the process of making significant changes to their regulations: Europe is in fact transitioning …

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