PRISYM ID to Exhibit at the European Medical Device Regulation Conference
PRISYM ID is exhibiting at the upcoming European Medical Device Regulation (MDR) Conference on 13th – 14th July in Arlington, VA.
With the EU Medical Device Regulation’s recent publication, the industry is currently analyzing gap assessment strategies to have a clear perspective of areas impacting medical device organizations. With provisions spanning all levels of device companies, the new regulation must be carefully interpreted and understood, in order to ensure a smooth transition in time and on budget.
EU MDR is being viewed as an extension of the FDA’s UDI (Unique Device Identification), but also a ‘step up’. However, it’s more detailed and more complex due to the local language requirements needed for Europe. Organizations - having just completed the hurdles of UDI compliance – need to embrace the lessons learnt and incorporate them into their labeling strategy to make bridging the gap easier in this new legislative landscape.
PRISYM ID is a market leader for label management solutions and can help you. For more information about PRISYM ID and to arrange a meeting during the event, please contact email@example.com