PRISYM ID to Exhibit at the UDI 2017 Conference in Baltimore
We are exhibiting at the Unique Device Identification (UDI) Conference in Baltimore, Maryland on the 7/8th June 2017, stand 4.
As the U.S. FDA UDI rule moves into its fourth year and with three of the four major compliance dates passed already, some manufacturers are now recognizing the value of doing more than just what is required by the regulation.
Throughout the event, workshops and keynote speakers will discuss issues ranging from UDI compliance, Master Data Management and Governance.
At last year’s event, where PRISYM ID also participated, there was lots of discussion about vision systems and how they can automate label inspection, post-print. This is a smart move for companies aspiring to achieve zero defect labeling; organizations are investing a huge amount of time and money to ensure labels are UDI compliant – so why risk an FDA recall or warning letter by potentially bringing in human error?
PRISYM ID is delighted to announce that, since last year’s event, it has launched a new automated print inspection module in addition to its renowned, flagship solution, PRISYM 360, to further transform global Label Lifecycle Management.
Visit PRISYM ID on stand 4 for a conversation about labeling challenges in the industry, including vision systems and the new EU MDR .
For more information about PRISYM ID and to arrange a meeting during the event, please contact email@example.com or call +1 508 948 6100