GMDN 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...