With a database of more than 15,000 strains VITEK® MS improves clinical decision-making for infectious diseases.
Canada
bioMerieux Receives FDA Clearance for Expanded Use of VIDAS® B•R•A•H•M•S PCT™ Test for Managing Sepsis Patients with Elevated Risk of Mortality
01 July, 2016
Tracking PCT – a biomarker for bacterial infections – over time provides strong indication of likely mortality, enabling physicians to personalize care for high-risk patients.
bioMérieux acquires Hyglos
01 June, 2016
bioMérieux acquires Hyglos and expands its offering to the detection of endotoxins in pharmaceutical products.
bioMérieux and the Lyon Civil Hospitals strengthen their collaboration
31 May, 2016
bioMérieux and the Lyon Civil Hospitals strengthen their collaboration and expand their partnership to include Claude Bernard University Lyon 1 Two joint research laboratories focused on a common goal: advancing medical research for the benefit of patients.
bioMérieux – First-Quarter 2016 Business Review
20 April, 2016
bioMérieux, a world leader in the field of in vitro diagnostics, today released its business review for the three months ended March 31, 2016.
bioMérieux – 2015 Financial Results
02 March, 2016
The Board of Directors of bioMérieux, a world leader in the field of in vitro diagnostics, met yesterday under the chairmanship of Jean-Luc Belingard and approved the consolidated financial statements for the year ended December 31, 2015.
BioFire’s FilmArray® Meningitis/Encephalitis Panel gets CE marked
26 January, 2016
FilmArray® expanded menu, with a fourth panel, is the largest available on a molecular biology multiplex platfom.
Fourth-Quarter 2015 Business Review
21 January, 2016
BioFire Submits Special 510(k) Application to the FDA for the use of FilmArray® Torch, the New High Throughput FilmArray® System with FilmArray® Respiratory Panel
12 January, 2016
bioMérieux, a world leader in the field of in vitro diagnostics, today announced that BioFire Diagnostics, LLC, its molecular biology affiliate, has submitted the FilmArray® Torch to the U.S. Food and Drug Administration (FDA) for special1 510(k) clearance for use with the FilmArray® Respiratory Panel (RP).