Medicines and Healthcare products Regulatory Agency

Brexit, MHRA
By  Sophie Porter 02:09 am January 6, 2021
Following its recent departure from the EU, the UK has introduced a new medical device information system (MDIS) that requires all medical devices available on the UK market to be registered with the Medicines and Healthcare products Regulatory Agency (MHRA) using official global medical device nomenclature (GMDN). The new system came into effect on 1 January 2021, with certain devices allowed a...
By  Brian Dolan 04:54 am September 1, 2010
Is wireless health regulation just as grey in the UK and other parts of Europe as it is in the US? "It's much easier to develop technology than it is to get permission to use it," Peter Bentley, the inventor of an iPhone app that supposedly turns the device into a stethoscope, told the UK's Guardian in a recent interview. Bentley, a researcher at the University College London, believes that...