QIAGEN announced plans to relocate its QIAstat-Dx operations in Barcelona to a new, state-of-the-art facility in Esplugues de Llobregat by early 2026. This move is part of a multi-year investment to enhance its syndromic testing solutions, including the QIAstat-Dx system, which identifies illnesses such as respiratory, gastrointestinal, and meningitis/encephalitis conditions.
The new 8,000-square-meter site will house Research & Development, Manufacturing, Sales, Marketing, Quality Assurance, and Regulatory Affairs. It will also serve as a hub for innovation in microfluidics and assay development. Designed for energy efficiency, the facility has achieved LEED Platinum Certification and will feature advanced digitalized production lines.
QIAstat-Dx utilizes cost-effective, single-use cartridges with multiplex real-time PCR technology to deliver results within an hour. The system has FDA-cleared panels for respiratory, gastrointestinal, meningitis, and encephalitis pathogens, alongside CE-marked panels under the European IVDR framework. QIAstat-Dx is also advancing into precision medicine, with partnerships with Eli Lilly and AstraZeneca focusing on genotyping for genomically targeted therapies.
Barcelona’s robust scientific ecosystem and local expertise—QIAstat-Dx originated from a Barcelona-based startup acquired by QIAGEN in 2018—make it an ideal location. The new site will expand diagnostic capabilities to address a broader range of pathogens, such as those causing urinary tract infections and blood culture identification, while supporting decentralized testing.
“QIAstat-Dx proved invaluable during COVID-19 and continues to address critical healthcare needs,” said Thierry Bernard, CEO of QIAGEN. "This expansion reinforces our commitment to advancing diagnostic solutions in infectious diseases and beyond." The facility will also support innovations in chronic diseases like neurodegenerative, metabolic, and inflammatory conditions, further strengthening QIAGEN’s diagnostic footprint.