PRISYM ID Exhibit at the Annual 2018 UDI Conference
We are exhibiting at the Unique Device Identification (UDI) Conference in Baltimore, on the 24th and 25th April 2018.
The 2018 UDI Conference attracts medical device manufacturers, distributors, GPO’s, and hospital systems that are impacted by the regulation. Manufacturers facing the UDI requirement should attend to understand the UDI rule and how to implement from the point of manufacturing and out to the customers. Whilst others can learn about implementing the UDI rule as a reseller and putting UDI to work in a hospital setting.
Visit PRISYM ID on stand 4 for a conversation around UDI, the challenges it presents in the industry and the new EU MDR. The introduction of UDI requirements into the EU is good news for organizations that are already along the pathway of adopting systems and processes to support FDA UDI compliance. However, for those that aren’t – and indeed those that may have made only basic adjustments to their labeling infrastructure.
Come and grab a copy of our latest EU MDR Whitepaper that sets out what exactly companies can learn from the current process of adapting systems to comply with FDA UDI regulation. For many, this has been a long and turbulent journey, therefore PRISYM ID guide organizations to face up to the challenges and learn from these experiences.