A US-based dental equipment and dental consumables manufacturer approached Freyr for Medical Writing services while updating its existing Clinical Evaluation Reports (CER) for some of its devices. The scope included EU MDD compliance for a few devices and transition to EU MDR compliance for other devices. As dental products require exclusive data mining, it was challenging for the client to compile and update its CER in a short time frame.
Download the case study to decode how Freyr managed to compile compliant CERs as per the requirements of the latest EU MDR and EU MDD.
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