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[Whitepaper] Checklist – Top MDR questions

In 2017 the Medical Devices Regulation (MDR) was published and marked the start of a four-year journey of transition from MDD to AIMDD. From the 26th of May 2021, the MDR will be fully applicable. During the transition, the manufacturers should have informed themselves and took into consideration the changes and certificates that are needed according to the new Regulation. In general, the MDR affects the industries of manufacturing, distribution or procuration of medical devices. It is good to be marked that no existing requirements have been removed. However, the process of transition is complex and a whole new line of questioning opens up…

 

To continue reading, download the whitepaper now by filling the fields below and get the answers to the top frequent asked question regarding the implementation of MDR!

 



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