The Transitional Measures Task Force, established under the Competent Authorities for Medical Devices groups (CAMD) to help roll out the EU Medical Devices and IVD Regulations, has finalized its first Q&A paper on implementation matters.
While no further details have emerged, the paper, Medtech Insight understands, has been endorsed by the new European Commission's Medical Devices Coordination Group (MDCG) and will soon be published.
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