Perspectives for reliable diagnostics: planning certainty until 2029
In June 2026, Euroimmun received official confirmation from TÜV Rheinland LGA Products GmbH that all of its in vitro diagnostic devices currently on the market under Directive 98/79/EG (IVDD) may continue to be marketed in the European Union. This confirmation applies to all devices for which Euroimmun had submitted a corresponding application based on EU […]



