Webinar by GS1 and Softgroup: Meeting UDI requirements for Medical Devices and In-vitro Devices
The deadline for implementation of traceability solutions for Medical Devices and In-vitro Devices is just around the corner. However, the MDR and IVDR regulations raise certain questions and challenges for manufacturers, importers, and authorized representatives.
SoftGroup and GS1 Bulgaria have teamed up to provide a compact and understandable overview of the most important regulatory updates as well as the specific UDI requirements.
When: 26th November 2020, at 10 a.m. EEST