This webinar is part of the series 'Ready and Resilient for the Respiratory Season', delivered by Hologic. Dr. Koeller (University Medical Centre, Institute for Medical Microbiology, Rostock, Germany) will explore In Vitro Medical Devices Regulation (IVDR) in the context of Laboratory Developed Tests (LDTs), and their compliance with IVDR.

As we move from pandemic to endemic COVID-19, Dr. Koeller will present on his approach to rapid response to the need of new diagnostics for emerging threats, whilst efficiently navigating the In Vitro Medical Devices Regulation (IVDR) requirements. 

TOPICS COVERED

Laboratory Developed Tests (LDTs) and the coming of age of IVDR.

WHO SHOULD ATTEND?

Biomedical scientists working in public and private laboratories with an interest in Laboratory Developed Tests (LDTs).

SPEAKERS

• Dr Daniele Gaudiosi, senior product manager Hologic
• Dr Oostrerlaken, Scientific affairs manager, Hologic
• Dr. Koeller, University Medical Center, Institute for Medical Microbiology, Rostock, Germany

For more information, please contact [email protected].