Making Sense of IVDR for LC-MS

The 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 IVD landscape, as well as affecting the laboratories using their own in-house testing - “Laboratory Developed Tests” (LDTs).

This webinar is recommended for the professionals who would like to learn more about the impact of IVDR on LC-MS/MS laboratories using LDTs.

Key learning objectives

  • 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?

Who should attend?

  • Professionals interested in the IVDR topic, heads of clinical laboratories, principal investigators, lab owners, and researchers at LC-MS laboratories

Certificate of attendance
All webinar participants can request a certificate of attendance, including a learning outcomes summary, for continuing education purposes.

Speakers

Magali Wolff
Magali Wolff
Head of Global Reagent Marketing & Support, Tecan, Hamburg

Moderator

Dora Wells
Dora Wells
Content Creator, SelectScience

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