PRISYM ID Exhibit at the Annual 2019 UDI Conference
PRISYM ID will be attending and exhibiting at this year’s UDI Conference in Baltimore, Maryland on 11th and 12th June 2019.
The UDI Conference will provide a forum for the FDA to discuss the details of the Final UDI Regulation and the Global UDI Database (GUDID) Guidance, so those impacted understand the components, know how to comply with the new requirements, and are able to develop their own implementation plan.
The conference will attract medical device manufacturers, distributors, GPO's, and hospital systems that will be affected by the regulation. Attendees will have regular access to the UDI exhibit hall during the Conference to explore various products and solutions within the industry.
For increased traceability, transparency and security, Unique Device Identification (UDI) is introduced in Europe through MDR and IVDR. This means that all medical devices sold in Europe will need to bear an UDI-marking on the product and labels as well as being registered in the EUDAMED database.
Come by Stand 16 to discuss with the PRISYM ID team the labeling implications of EU MDR, lessons learned from UDI; and how our labeling solution can help you achieving regulatory compliance.
While there, don’t forget to grab a copy of our infographic: