At Certest, we continue to make progress in adapting our portfolio to the European In Vitro Diagnostic Medical Devices Regulation (IVDR). We currently have 112 CE IVDR-certified products, representing a total of 1,443 references.
This latest expansion marks an increase from the previously certified 64 products and 776 references, allowing us to offer an increasingly broad range of diagnostic solutions that comply with European regulatory requirements.
CE IVDR certification establishes strict requirements for the safety, performance, and quality of in vitro diagnostic devices, aiming to ensure their reliability and protect patients and users.
With these advances, Certest continues to work towards aligning its portfolio with European regulatory standards and providing laboratories, healthcare professionals, and distributors with diagnostic solutions that meet their needs.
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