E.g., 11/22/2024
E.g., 11/22/2024

BIOFIRE® Respiratory Panel 2.1 plus with SARS-CoV-2 is CE marked

15 Luglio, 2020

CE marking of bioMérieux serology tests for SARS-CoV-2 on VIDAS®

27 Maggio, 2020

bioMérieux serology tests for SARS-CoV-2 on VIDAS® undergo validation preceding imminent launch 

06 Maggio, 2020

BIOFIRE® Respiratory Panel 2.1 (RP2.1) with SARS-CoV-2 obtains FDA Emergency Use Authorization 

04 Maggio, 2020

COVID-19: comunicazione di A.Mérieux, CEO di bioMérieux 

31 Marzo, 2020

bioMérieux receives Emergency Use Authorization for BIOFIRE® COVID-19 test

24 Marzo, 2020

First-Quarter 2020 Business Review

24 Marzo, 2020

First of 3 diagnostic tests for  SARS-CoV-2 coronavirus available from bioMérieux

11 Marzo, 2020

bioMérieux – 2019 Financial Results

14 Gennaio, 2020

bioMérieux submits enhanced BIOFIRE® BCID2 Panel for FDA clearance

14 Gennaio, 2020

bioMérieux, a world leader in the field of in vitro diagnostics, announces that BioFire Diagnostics, its molecular biology affiliate, has submitted to the Food and Drug Administration for 510(k) clearance of the BIOFIRE® Blood Culture Identification 2 (BCID2) Panel. The BIOFIRE® BCID2 Panel includes several additional pathogens, an expanded list of antimicrobial resistance genes, and many revised targets compared to the existing BIOFIRE® BCID Panel.d about 9,800.

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