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EVAMED is a specialized Contract Research Organization (CRO) focused on the clinical evaluation of medical devices and in vitro diagnostics. Based in France, the company provides comprehensive services including clinical trial design, regulatory strategy, data management via proprietary eCRF tools, and clinical evaluation reports (CER). EVAMED supports manufacturers in navigating complex European regulations such as the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). Their expertise spans various therapeutic areas, ensuring that medical innovations meet safety and performance standards for market access.
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