Hi Readers,
I started hearing about EU MDR in one of the project, and I am not sure what is its relation to SAP GTS and the configuration involved into it.
When I checked online it is EU Medical Devices Regulation and how it is important in EU, but could not related to GTS. Can some one please help me what we are looking at from GTS end?
What we need to consider when working with EU MDR?
Thanks,
Alex Kid
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