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MDR replaces MDD: New European Medical Device Regulation
The purpose of the MDR is to significantly improve the quality, safety and reliability of medical devices and market surveillance mechanisms for medical devices.
- The audit successfully demonstrated that MEDDI hub as is prepared for the MDR rules
- The MEDDI app is in compliance with the MDR regulation
it is a commitment, not an obligation
Compliance with the criteria according to the MDR is an obligation for us, not just a necessary duty
We are committed to ensuring that all our solutions meet the relevant requirements of the MDR in accordance with the relevant transition periods. From now on, forever.
- We continuously verify quality with independent audits
- We constantly pay attention to the safety and reliability of our applications
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MEDDI
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MEDDI hub a.s.
Na Florenci 2116/15, Nové Město
110 00 Praha 1
06230458
CZ06230458
+420 603 807 777
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