z.B. 11/24/2024
z.B. 11/24/2024

bioMérieux Completes its VIDAS® Hepatitis Panel with a New Test for the Diagnosis of Hepatitis C

03 Mai, 2012

bioMérieux, a world leader in the field of in vitro diagnostics, announces the launch of VIDAS® Anti-HCV for the detection of the hepatitis C virus (HCV). With this new CE marked test, VIDAS® now has a complete hepatitis menu with tests for A, B and C viral hepatitis.

bioMérieux’s Myla® Named as Finalist in the 2012 Medical Design Excellence Awards

12 April, 2012

A world leader in in vitro diagnostics, bioMérieux today announced that its microbiology middleware, Myla® has been selected as a finalist in the In Vitro Diagnostics category of the Medical Design Excellence Awards (MDEA)competition. Myla is an innovative microbiology middleware solution that offers consolidated interfacing, workflow optimization and information management. Myla is browser-based and consolidates information that can impact patient care and efficiency from ID/AST and blood culture testing in a single interface for the LIS. Users can access Myla remotely from anywhere on their network.

bioMérieux Initiative to Support European Antibiotic Awareness Day

18 November, 2011

As the world leader in microbiology and a pioneer in diagnostics for antimicrobial resistance detection and susceptibility testing (AST), bioMérieux actively supports the annual European Antibiotic Awareness Day, organized today by the ECDC.1 bioMérieux subsidiaries throughout the world are providing educational tools for healthcare professionals to help increase public awareness about this serious issue.

bioTheranostics’ CancerTYPE ID® Linked with Improved Clinical Outcome and Longer Survival

08 November, 2011

bioTheranostics, Inc., a bioMérieux company that develops innovative oncology diagnostic tests to drive personalized treatment, today announced clinical study findings that link CancerTYPE ID® molecular testing with improved patient outcome. Patients in which CancerTYPE ID predicted a colorectal site of origin that subsequently received site-specific therapy had a median survival three times that of what has been reported in patients treated empirically for cancer of unknown primary (CUP). These results make CancerTYPE ID the only marketed molecular cancer classifier to demonstrate therapeutic response and patient benefit based on molecular tumor profiling.

Pioneering diagnostics