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BioWorld - Friday, May 1, 2026
Home » Keywords » Biomérieux SA

Items Tagged with 'Biomérieux SA'

ARTICLES

Mycobacterium tuberculosis

Oxford Nanopore, Biomérieux launch Ampore-TB test

Nov. 5, 2025
By Shani Alexander
Oxford Nanopore Technologies plc and Biomérieux SA launched Ampore-TB, a research use only test that can rapidly detect mutations linked to antimicrobial resistance in tuberculosis. With multidrug-resistant TB affecting an estimated 400,000 people annually and increasing risks of morbidity and mortality, this assay could help with earlier diagnosis of drug resistance in patients.
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Art concept for antimicrobial research

FDA clears Biomérieux’s Vitek Compact antimicrobial resistance system

March 25, 2025
By Shani Alexander
Biomérieux SA recently received U.S. FDA 510(k) clearance for its Vitek Compact Pro, a system for microorganism identification and Antibiotic Susceptibility Testing. The company hopes that the system will help clinical laboratories combat antimicrobial resistance and diagnose infectious diseases as well as support industrial laboratories in identifying contaminants to ensure consumer safety.
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Illustration showing layers of the meninges between the skull and brain

FDA clears fourth Qiagen test in 2024

Nov. 5, 2024
By Annette Boyle
Qiagen NV added to its growing roster of panels cleared by the U.S. FDA in 2024 with the agency’s nod for its Qiastat-Dx Meningitis/Encephalitis assay. The clearance validates Qiagen’s strategy of developing rapid tests specifically for the U.S. market and builds on the respiratory, gastrointestinal and central nervous system tests already available.
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Blood cells and bacteria

Abionic’s test enters increasingly competitive sepsis fray

Oct. 31, 2024
By Annette Boyle
Abionic SA received U.S. FDA 510(k) clearance for its in vitro diagnostic Capsule pancreatic stone protein (PSP) sepsis test. Produced by the pancreas and immune cells, PSP provides an early biomarker for sepsis that could push back detection of deadly condition by 24 to 48 hours.
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Qiastat-Dx Respiratory SARS-CoV-2 panel, hospitalized patient in background
In vitro diagnostics on the rise

COVID-19 puts IVDs in the spotlight, but global investment seeks to bolster their use elsewhere

Dec. 7, 2021
By Catherine Longworth
Due to COVID-19, diagnostics are in the limelight, and public and private investors are watching how the pandemic may impact the in vitro diagnostics (IVD) market in the future. As the sector receives an influx of investment, companies will be in strong positions to expand their portfolios. So, with 2022 around the corner – what are the investment trends to watch?
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Europe under magnifier/petri dish with coronavirus

European IVD med-techs upping efforts to launch rapid COVID-19 screening tests

March 31, 2020
By Bernard Banga
PARIS – Europe has turned into the epicenter of the coronavirus pandemic, seeing more than 50% of the cases observed worldwide. In fact, whereas the COVID-19 pandemic has begun declining in China where it originated, there are 400,000 cases of coronavirus worldwide, including more than 200,000 infected by SARS-CoV-2 in the 55 sovereign states in continental Europe, where they are mourning more than 18,000 deaths.
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