Understanding the Classification System for In Vitro Diagnostic Devices under the EU IVDR 2017/746

Blog Image
Understanding the Classification System for In Vitro Diagnostic Devices under the EU IVDR 2017/746

In Vitro Diagnostic (IVD) devices play a crucial role in healthcare by providing valuable information for disease diagnosis, patient monitoring, and treatment decisions. The European Union's In Vitro Diagnostic Regulation (IVDR) 2017/746 introduced a new classification system for IVDs.