The GMDN Agency is responsible for the Global Medical Device Nomenclature (GMDN) used to identify medical devices.
22 Dec 2020 - The MHRA’s predecessor, the MDA, was a driving force in the creation of the GMDN in the 1990s and has used it on a voluntary basis ever since. In 2018 the MHRA …
07 Dec 2020 - The MHRA have published new guidance for companies that place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets from 1 Jan…
04 Dec 2020 - On 1st December 2020 the European Commission has made available the Actor registration module. It is the first of six EUDAMED modules that will be needed before…