PRISYM ID to exhibit at the 7th Annual EU Device & Diagnostic Regulation Conference

PRISYM ID to exhibit at the 7th Annual EU Device & Diagnostic Regulation Conference

PRISYM ID, is exhibiting at the 7th Annual EU Device & Diagnostic Regulation Conference in Brussels, Belgium on the 25/26th September 2017.

The conference’s in-depth focus on the MDR & IVDR will ensure a holistic approach to current changes in the European Union, providing participants with a plethora of enlightening solutions to complex regulatory transitions. High-level presentations and tracked interactive session formats will allow delegates from across the industry to engage in hands-on activities with peers and industry thought leaders.

It’s important to adopt an MDR solution that is not only designed to tackle the regulatory challenges of today, but can also provide a platform to address the evolving needs of tomorrow.

PRISYM ID will undertake a presentation on 25th September from 12:30 – 12:45pm. The presentation will focus on EU MDR, whilst highlighting its flagship, label life-cycle management solution, PRISYM 360.

At a time of increased scrutiny and enduring regulatory change, the proprietary solution gives organizations complete label integrity to meet the compliance requirements of FDA and EU regulations – as well as the scope to adapt to emerging regulations as and when they occur.

For more information about PRISYM ID and to arrange a meeting during the event, please contact info@prisymid.com or call +44 (0)118 936 4400

Watch back our webinar: Bridging the Gap – How to be EU MDR Labeling Compliance Ready by Using the Lessons Learnt from UDI