Making Sense of IVDR for LC-MS

The In Vitro Diagnostic Regulation (IVDR) is the European Union’s set of rules aimed at improving the quality, safety, and reliability of IVDs. This regulation is impacting the in vitro diagnostic landscape, as well as affecting the laboratories using their own in-house testing (“Laboratory Developed Tests” (LDTs)).

For professionals managing LDTs, finding relevant information and understanding the impact on your labs can be challenging. You are invited to watch the webinar, "Making sense of IVDR for LC-MS," which addresses these challenges by covering:

• What is IVDR and what are the timelines?
• Requirements for in-house tests (LDTs).
• Next steps for your lab.

This is an opportunity to stay ahead and ensure lab compliance with the latest regulations.