QIAGEN plans to relocate QIAstat-Dx operations to a new 8,000-square-meter site in Barcelona by early 2026, supporting syndromic testing for infectious diseases and precision medicine, with R&D, manufacturing, sales, marketing, and regulatory operations, featuring digitalized production lines and LEED Platinum certification, aiming to strengthen diagnostic capabilities and support partnerships with Eli Lilly and AstraZeneca. The system currently has FDA clearance for four panels and CE-marking for two panels under IVDR.