PRISYM ID to Exhibit at the European Medical Device Regulation Conference

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 info@prisymid.com