Unser Partner DHC lädt ein zur SAP Life Sciences Webkonferenz mit dem Fokus „UDI mit SAP für den Mittelstand“. SAP, DHC und projektraum36 zeigen gemeinsam in der Webkonferenz, wie Sie die FDA- und die neuen europäischen MDR-Anforderungen zur Unique Device
Together with our Partners SAP, DHC and NNIT we continue our collaborative Webinar series on EU Medical Device Regulation (MDR) and Unique Device Identification (UDI). It is embedded into SAP´s quarterly Life Sciences Regulatory Roundtable. Get an update on recent
Together with our Partners SAP and NNIT we invited to a collaborative Webinar on Unique Device Identification (UDI) as central part of the EU Medical Device Regulation (MDR). Learn, how EU MDR affects you as a Medical Device Manufacturer and
Manufacturers of Medical Devices must take action now in order to submit their Product Master Data to Unique Device Identification (UDI) Databases worldwide. After the US Food and Drug Administration (FDA) the EU will follow with its Medical Device Regulation (MDR), becoming