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It's Not All Over Once EU Medtech Regulations Are Adopted, Says EDMA Chief

This article was originally published in SRA

Executive Summary

While the medtech sector focuses intently on the current series of trilogues between the European Commission, the Council of the European Union and the European Parliament on the future Medical Device Regulation and IVD Regulation, it is easy to forget that when the texts are adopted they will still not represent the full picture1. Some of the most significant details will emerge in the delegated and implementing acts that will follow.