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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.
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QIAGEN (NYSE: QGEN) has announced significant enhancements to its QIAcuity digital PCR (dPCR) systems, including 13 new kits and assays for AAV viral titer and host cell DNA quantification, aimed specifically at biopharma applications. With over 1,000 cumulative placements since launch in late 2020, the updates also feature an upgraded software suite for GMP compliance. These developments are designed to improve efficiency and expand the utility of QIAcuity for biopharma customers, enhancing drug development processes.
QIAGEN N.V. reported Q2 2022 net sales of
QIAGEN's Clinical Insights (QCI) platform has surpassed three million analyzed cases, reflecting a remarkable annual growth rate of over 35%, equivalent to 700,000 new cases. This software has outperformed competitors, analyzing five times more cases than other offerings. QCI integrates advanced Augmented Molecular Intelligence, enabling healthcare providers to enhance NGS testing reliability. QIAGEN aims to continue expanding its comprehensive solutions to meet the growing demand in the genetic analysis sector.
QIAGEN N.V. (NYSE: QGEN) will release its second quarter 2022 results on Wednesday, July 27, after 22:05 Frankfurt time. A conference call is scheduled for Thursday, July 28, at 15:30 Frankfurt time. Participants can join the call via callback connection, phone, or audio webcast. The company provides innovative solutions for molecular diagnostics and life sciences, serving over 500,000 customers globally. For further details, visit qiagen.com.
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QIAGEN (NYSE: QGEN) receives validation from the CDC for its QIAcuity digital PCR system for wastewater surveillance, marking a shift from traditional qPCR methods. This endorsement allows public health labs to utilize QIAcuity for detecting 30 pathogens, including SARS-CoV-2. Previously, QIAcuity was adopted in public health labs across 70% of U.S. states, enabling rapid results in just two hours. The CDC will now exclusively accept data from QIAcuity and another approved digital PCR platform, reinforcing QIAGEN's role in infectious disease monitoring and expanding its applications beyond COVID-19.
QIAGEN has launched its QIAwave nucleic-acid extraction kits, achieving a 35% lower environmental impact compared to standard kits. The products are the first in the industry to receive the ACT Environmental Impact Factor Label from
QIAGEN has launched the QIAstat-Dx Rise, an advanced automated syndromic testing system receiving CE-marking, enabling up to 56 tests in an eight-hour shift. The system enhances the capacity for detecting multiple pathogens simultaneously, crucial for high-demand medical facilities. Key updates include an expanded QIAstat-Dx Respiratory SARS-CoV-2 Panel that now tests for 23 pathogens, including Chlamydophila pneumoniae, and a new Gastrointestinal Panel with improved performance. Additionally, a software update enhances cybersecurity and connectivity for the QIAstat-Dx systems.
QIAGEN has acquired a 96% stake in BLIRT SA, enhancing its capabilities in recombinant enzymes and molecular biology reagents. BLIRT, based in Poland, specializes in producing essential proteins and enzymes for diagnostics, generating under $10 million in sales in 2021. This acquisition aims to bolster QIAGEN's sample technologies business, expand global production, and enhance R&D capacities. The deal is expected to close in Q2 2022 and will not materially impact QIAGEN's financial outlook for the year, as previously stated.
QIAGEN N.V. announced Dr. Eva Pisa as a proposed new member of the Supervisory Board, enhancing leadership in the Life Science and Molecular Diagnostics sectors. All current board members will stand for re-election at the Annual General Meeting scheduled for June 23, 2022, in Venlo, Netherlands. Dr. Pisa's experience includes roles at Sangtec Molecular Diagnostics and Roche Diagnostics, offering valuable insights into health diagnostics. This strategic move aligns with QIAGEN's commitment to value creation for stakeholders in the Life Science and Molecular Diagnostics markets.