Future proofing your flow cytometry panel under IVDR


IVDR is a marathon, not a sprint. We’ll help you go the distance. Like many other ideas that are intended to improve existing products or procedures, the new European IVD Regulation (IVD-R) 2017/746 road is paved with good intentions. It will create a robust European-wide regulatory framework for improving patient diagnostics and safety but will also have a significant impact on clinical labs conducting Laboratory-Developed Tests (LDTs), such as flow cytometry panels, as those are now in the scope of the regulation.

In this webinar Pieter Bogaert, Senior Expert for Device Compliance at Qarad BV, to give an overview about the options clinical labs have to future proof their flow cytometry panels in the context of IVDR.

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