Ortho Clinical Diagnostics announces FDA approval of a diagnostic assay for the detection of antibodies to human immunodeficiency virus (HIV) types 1+2 (Anti-HIV 1+2) for use on the VITROS 5600 Integrated and VITROS 3600 Immunodiagnostic Systems.
Read MoreNanosphere Inc announced today it has received 510(k) clearance from the FDA for its influenza A & B and respiratory syncytial virus (RSV) test and the Verigene SP System, with complete sample-to-result automation.
Read MoreThis document provides interim guidance for state and local health departments, hospitals, and clinicians participating in surveillance activities regarding which patients to prioritize for testing by RT-PCR for influenza surveillance.
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The FaBs Product Features and Benefits is available as a downloadable pdf – you will need Adobe Acrobat reader to view this. If you do not have Adobe Acrobat on your computer, you can download it for free from Adobe.com.
Read MoreOrion Genomics today announced that it has entered into a multi-year collaboration and license agreement with the molecular diagnostics unit of Novartis Pharma AG.
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