E.g., 07/25/2021
E.g., 07/25/2021

bioMérieux – Business Review del primo trimestre 2021

27 Aprile, 2021

bioMérieux, leader globale nella diagnostica in vitro comunica la business review per il trimestre conclusosi il 31 Marzo 2021.

bioMérieux announces the CE marking of 3 dengue immunoassays on VIDAS®

07 Aprile, 2021

bioMérieux, a world leader in the field of in vitro diagnostics, announces the CE marking of its innovative and fully-automated assays to diagnose dengue infection: VIDAS® DENGUE NS1 Ag VIDAS® Anti-DENGUE IgM VIDAS® Anti-DENGUE IgG

bioMérieux announces the CE marking of TB IGRA® test on VIDAS®  

24 Marzo, 2021

Today marks World Tuberculosis (TB) Day and bioMérieux, a world leader in the field of in vitro diagnostics, announces the CE marking of its innovative and fully-automated test VIDAS® TB IGRA (Interferon-Gamma Release Assay) to diagnose latent TB infection.

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

18 Marzo, 2021

Marcy l’Étoile (France) – bioMérieux, a world leader in the field of in vitro diagnostics, today announced that BioFire Diagnostics, its subsidiary specialized in molecular syndromic infectious disease testing, has received U.S. Food and Drug Administration (FDA) De Novo authorization for the BIOFIRE® RP2.1 Panel. 

bioMérieux annuncia la marcatura CE del test NEPHROCHECK® su VIDAS®

03 Febbraio, 2021

Marcy l’Etoile, Francia – 3 Febbraio, 2021 – bioMérieux, leader globale nella diagnostica in vitro comunica la marcatura CE dell’innovativo test  NEPHROCHECK® in grado di individuare lo stress renale nei pazienti a rischio di danno renale acuto (AKI).

bioMérieux announces the expansion of the CE marking of its molecular biology ARGENE® SARS-CoV-2 diagnostic test to include saliva specimens.

17 Novembre, 2020

Marcy l’Etoile, France – November 16, 2020 – bioMérieux, a world leader in the field of in vitro diagnostics, has announced the expansion of its ARGENE® range for the detection of SARS-CoV-2. As a complement to nasopharyngeal swab specimens, the singleplex SARS-CoV-2 R-GENE® real-time PCR test may now be used on saliva and oropharyngeal (throat) swab specimens for the detection of the virus that causes COVID-19. This development helps optimize laboratory workflows.

First-Half 2020 Results

02 Settembre, 2020

Pioneering diagnostics