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The CAMD (Competent Authorities for Medical Devices) published on their web site 2 documents related to FAQs to the transitional provisions of MDR and IVDR.

datesjanv2015http://www.camd-europe.eu/media-centre

By | 2018-06-29T11:19:13+00:00 January 24th, 2018|news|0 Comments

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