The GMDN Agency will be presenting at UDIs and Traceability for Medical Devices Forum in Brussels, Belgium on 17-18 May 2017
Discover key lessons learned from FDA Class II implementation in the North American regions and how these lessons can be applied to European UDI implementation. Prepare your organisation for the new European UDI guidelines.
Ensure your Master Data Management is set up for GUDID, EUDAMED and optimal organisational support.
More information at www.udisandtraceability.com