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Making sense of IVDR for LC-MS

RECORD | Already taken place Th, 18.4.2024

In this webinar you will learn what is IVDR and what are the timelines, what are the requirements for in-house tests, and what are the next steps for your lab.

Go to the webinar

SCIEX: Making sense of IVDR for LC-MS

In Vitro Diagnostic Regulation (IVDR) is the European Union’s new set of rules aimed at improving the quality, safety and reliability of IVDs. The new regulation is impacting the in vitro diagnostic landscape, affecting laboratories using their own “Laboratory Developed Tests” (LDTs) and those compliant with certain accreditation e.g. standard EN ISO 15189.

In this webinar you will learn:

What is IVDR and what are the timelines
What are the requirements for in-house tests (LDTs)
What are the next steps for your lab

Presenter: Fabian Reijn (Diagnotix)

Presenter: Magali Wolff (Tecan)

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Making sense of IVDR for LC-MS

Related content

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