The UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) embeds Global Medical Device Nomenclature (GMDN) in Public Access Registration Database (PARD) for Enhanced Medical Device Regulation.
In a significant development for medical device regulation, the Global Medical Device Nomenclature (GMDN) has joined forces with the UK’s Medicines and Healthcare Products Regulatory Agency (MHRA) to strengthen the functionality of the MHRA’s Public Access Registration Database (PARD).
The integration of GMDN within PARD aims to improve patient safety, streamline the classification, promote transparency, and enhance accessibility to vital medical device information.
