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Abstract
Now that the IVDR explicitly regulates in-house devices or "Laboratory Developed Tests" (LDTs), the selection of properly CE-labelled devices is becoming increasingly important for laboratories. In this webinar, we will explain the classification of devices under IVDR and what it means for manufacturers, users and patients. We will also show you how the varvis® genomics platform meets the requirements and give you an exclusive insight into our software. We also plan enough time to answer all your questions.