Welcome to our dedicated page for Qiagen news (Ticker: QGEN), a resource for investors and traders seeking the latest updates and insights on Qiagen stock.
Qiagen N.V. (QGEN) delivers essential molecular testing solutions powering advancements in healthcare, research, and applied sciences. This dedicated news hub provides investors and professionals with authoritative updates on Qiagen's innovations in sample preparation, automated diagnostics, and bioinformatics.
Access real-time announcements including earnings reports, regulatory milestones, and strategic partnerships. Our curated collection features press releases on product launches, clinical study collaborations, and technology integrations across molecular diagnostics and life sciences.
Key updates cover Qiagen's expanding portfolio for precision medicine, infectious disease testing, and next-generation sequencing workflows. Track developments in critical areas like companion diagnostics and laboratory automation solutions serving global healthcare providers and research institutions.
Bookmark this page for streamlined access to Qiagen's official communications. Stay informed about the company's progress in transforming biological insights into actionable results across 40+ countries.
QIAGEN has received European IVDR certification for its QIAGEN Clinical Insight Interpret, a clinical decision support software for next-generation sequencing (NGS) in oncology and hereditary applications. This certification ensures the platform complies with the EU's regulatory framework, enhancing patient safety, data transparency, and traceability. The software has already processed over 4 million NGS patient test cases globally. The certified version will be available in Europe by late 2024, facilitating faster and more accurate clinical decision-making.
QIAGEN has received FDA clearance for its QIAstat-Dx Respiratory Panel Plus, a syndromic test for diagnosing upper respiratory infections. The panel covers 21 viral and bacterial targets, delivers results in about an hour with minimal hands-on time, and provides access to Ct values and amplification curves. This technology aims to improve patient care, support antimicrobial stewardship, and reduce healthcare system burden. QIAGEN is expanding its testing menu, with a Gastrointestinal Panel under FDA review. The company also launched the QIAstat-Dx Analyzer 2.0, featuring cloud-based connectivity and remote result access, enhancing collaboration in healthcare.
QIAGEN partners with the FBI to develop a novel digital PCR assay for QIAcuity to enhance DNA analysis in forensics, improving accuracy, speed, and reliability in human identification. The collaboration aims to quantify DNA from human samples for forensic use, strengthening QIAGEN's leadership in human identification and forensics.
QIAGEN has launched QCI Secondary Analysis, a cloud-based software solution that enhances bioinformatics workflows for oncology and inherited disease applications. The software, integrated with QCI Interpret, enables high-throughput secondary analysis of clinical next-generation sequencing data, advancing precision medicine and making NGS testing accessible to smaller labs. The solution provides a secure and compliant environment for bioinformatics workflows, supporting all QIAGEN QIAseq panels.
QIAGEN reported its Q1 2024 results, showcasing net sales of $459 million with a 5% decline, but exceeded expectations with $462 million at constant exchange rates. The company's adjusted operating income margin rose to 25.7% from 25.6% in Q1 2023, with adjusted diluted EPS at $0.46, above the outlook of $0.44. Key growth drivers include double-digit CER growth in QuantiFERON and QIAstat-Dx, resulting in a positive outlook for 2024 with reaffirmed guidance of at least $2.0 billion in net sales and adjusted diluted EPS of at least $2.10 CER.
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