The biggest news for March when it comes to the implementation of the Medical Device and IVD regulations is, in fact, the ongoing lack of news, prompting questions about whether this means the European Commission may be planning to take some decisive action that could result in an extension of timelines, for example, particularly for the MDR.
The French and German industry associations issued a position paper in mid-March calling for the grace period for MDR products to be extended by two years for class III...
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