Since December 2022, European regulatory bodies have been working to enact Regulation 2023/607 to...
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Bringing medical devices to market is a process that often takes years. Manufacturers are required...
The Medical Devices Coordination Group (MDCG) has published guidance discussing the health...
The MHRA has extended the scope of UL International UK Limited’s approved body designation to...
The UK Life Sciences Council has issued a statement concerning their agreement to publish proposals...
The European Commission has proposed to extend the transitional periods of the Medical Devices...
Essential requirements are a common feature of medical device regulations around the world. At the...
Last September, the Medicines & Healthcare products Regulatory Agency (MHRA) launched a change...
The UK government has outlined plans to reduce the environmental impact and sustainability of...
On June 26 2022, the UK government published its response to the Medicines and Healthcare products...