The UK government is planning a substantial reform of the current regulatory framework for medical devices in the country. In response to the 2021 con...
UK Guidance update with MORE Submissions & Production API
The UK government has recently updated its guidance for CE marked medical devices in Great Britain with new information on MORE Submissions and Produc...
Crafting an Intended Purpose for Software as a Medical Device (SaMD)
Software as a Medical Device (SaMD) As a Software Medical Device (SaMD) manufacturer, you know that regulatory compliance is key to market success. De...
The UK and Switzerland have embraced the EU MDR extension!
The EU currently leads the way in regulatory standards, with the UK and Switzerland following suit. This is being done for valid reasons, as medical d...