Medical Devices conference, held in Munich, Germany on 28-29 January, was filled with sessions that dug into the minutiae of ...

Medical and Healthcare Products Regulatory Agency (MHRA) has released new guidance to help manufacturers meet UK medical ...

Medical devices are revolutionizing healthcare. These devices improve patient outcomes, from tracking and recording vitals to measuring glucose levels to supporting cardiac conditions. The future ...

The classification of medical devices are done at the state ... because their interpretation of the risk were different from the device manufacturers. Now, that ambiguity has been addressed ...

For those with Class IIa or above AI-related devices, compliance with the EU’s AI Act is likely to be akin to the EU MDR.