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June 29, 2021
Our freelancers have helped medical device manufacturers of all sizes achieve regulatory compliance. Speak to an expert directly for help with MDR gap assessment, CE transition, EU MDR compliance checklists, MEDDEV 2.7/1 rev 4, clinical evaluation reports, technical documentation, and more.
More information on our website:
https://www.kolabtree.com/services/eu-mdr-consulting/