PRISYM ID is talking about Best Practices for EU MDR and UDI Implementation at the Mediteq Forum 2018

PRISYM ID is talking about Best Practices for EU MDR and UDI Implementation at the Mediteq Forum 2018

PRISYM ID will present, alongside GS1, at the Mediteq Forum Seminar, on 13th November 2018, from 1 pm to 5 pm, in Goteborg, Sweden, Aktiviteten at Lindholmen Science Park.

For an 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. The seminar will discuss practical implications and lessons learnt for how to implement UDI, labelling and related data management, e.g information transfer to Eudamed.

Please see the program here

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Steve Ellison

Vice President EU Sales

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