QIAGEN Launches QIAcuityDx Digital PCR System For Clinical Testing In Oncology
Portfolio Pulse from Benzinga Newsdesk
QIAGEN has launched the QIAcuityDx Digital PCR System for clinical oncology testing, expanding its digital PCR portfolio into clinical diagnostics. The system is 510(k) exempt in the U.S. and IVDR-certified in Europe, offering precise DNA/RNA quantitation for cancer monitoring. QIAGEN plans to expand its application menu and has partnered with pharmaceutical companies for companion diagnostics development.
September 30, 2024 | 8:13 pm
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QIAGEN's launch of the QIAcuityDx Digital PCR System marks a significant expansion into clinical diagnostics, particularly in oncology. The system's regulatory approvals in the U.S. and Europe, along with partnerships for companion diagnostics, position QIAGEN for growth in precision medicine.
The launch of the QIAcuityDx system is a strategic move for QIAGEN, expanding its presence in the clinical diagnostics market. The system's regulatory approvals in key markets (U.S. and Europe) and its partnerships with pharmaceutical companies for companion diagnostics development are likely to drive demand and revenue growth. This positions QIAGEN well in the growing field of precision medicine, particularly in oncology, which is a high-growth area.
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