Live webinar of the Kern Experience
Master Data Management of the EU Medical Devices Regulation in SAP
A guest lecture by Ismail Demiralp, Europe IT Consulting GmbH
Since 26.05.2021, the Medical Device Regulation MDR 2017/745 of the European Commission is in application. This means that medical devices may only be placed on the market in accordance with the current UDI requirements and soon the UDI data will also have to be transmitted to EUDAMED.
Learn in this webinar how our UDI SAP EUDAMED add-on is the optimal solution for implementing the Medical Devices Regulation (MDR 2017/745 & IVDR 2017/746). The UDI data management in the add-on ranges from UDI data maintenance and data validation to data transmission to EUDAMED. Numerous functions such as UDI data upload and export, mass maintenance and the audit trail provide additional support for fast and efficient UDI data management.
You will receive this and other relevant information in this webinar.
(The webinar is held in German.)
Contact
If you have any questions in advance, please contact us by e-mail or telephone on +49 (761) 791 878-197.