Mittwoch, 24. August 2022 um 16 Uhr
We will discuss the pros & cons of the 3 options proposed by the EU Commission, leveraging our unique experience within the community of Medical Device and IVD manufacturers of all sizes confronted with this choice. This is not a simple decision since many contributing factors should be considered, and it will structure how you can most efficiently comply with the MDR / IVDR and other regulatory requirements.
Whether you’re a large user with thousands of UDIs or just have a couple of devices, you will understand the difference between the EUDAMED website, the manual upload of XML files into EUDAMED and the full integration M2M with EUDAMED and be able to take your decision with all the necessary information.
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KONTAKT:
KölnOnline
