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  • ABL SARS-CoV-2 Antibody Test Now Approved for Emergency Use by ANVISA in Brazil

    Aug 25, 2020

    We are pleased to announce that ANVISA approved the SARS-CoV-2 Antibody Test (colloidal gold immunochromatography) for Emergency Use in Brazil. Please contact us for more information.

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  • New Publication on DeepChek®-HCV Drug Resistance Assays and Software (Virology Journal)

    Jul 17, 2020

    Detection of low-level HCV variants in DAA treated patients: comparison amongst three different NGS data analysis protocols Caputo et al. Virology Journal (2020) 17:103 https://doi.org/10.1186/s12985-020-01381-3 Abstract Background: Notwithstanding the efforts of direct-acting antivirals (DAAs) for…

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  • ABL Appointed as the Exclusive Distributor of all NimaGen sequencing products for France, Belgium and Luxembourg

    Jul 15, 2020

    We are pleased to announce that Nimagen appointed ABL as its exclusive distribution partner for Sequencing Products in France, Belgium and Luxembourg. The partnership was formalized on March 17th 2020 and will help all labs involved in sequencing to get access to robust and cost-effective solutions…

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  • Advanced Biological Laboratories (ABL) Releases the First & Unique Commercial CE-IVD Registered COVID-19 rRT-PCR Assay Validated also for Human Saliva Specimens

    Jul 06, 2020

    Single well rRT-PCR assay, including highly sensitive detection of 2 targets and housekeeping internal control, with full automation   Luxembourg (Luxembourg), Metz (France), — July 06 — Advanced Biological Laboratories (ABL) announced today the CE-IVD marking of its UltraGene® Combo2Screen SARS-CoV…

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  • SARS-CoV-2 PCR Assay Now Approved for Human Saliva Specimens

    Jun 17, 2020

    First rt-PCR detection kit CE marked for nasopharyngeal and saliva samples. Improve COVID-19 management with non-invasive, open and sensitive assay.  Luxembourg (Luxembourg), Metz (France), — June 17 — Advanced Biological Laboratories (ABL) announced today the validation of its CE-IVD UltraGene® Com…

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  • Highly Satisfactory Accuracy for the UltraGene Combo2Screen SARS-CoV-2 Assay on the QCMD 2020 Coronavirus Outbreak Preparedness EQA Pilot Study

    May 29, 2020

    We are pleased to announce that the UltraGene Combo2Screen SARS-CoV-2 Assay has obtained Highly Satisfactory results (with a 100% accuracy for qualitative detection of all QCMD blinded samples, including with lowest viral load) in the context of the QCMD 2020 Coronavirus Outbreak Preparedness EQA Pi…

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  • Advanced Biological Laboratories Receives CE-IVD Registration for its UltraGene Combo2Screen SARS-CoV-2 Assay

    May 21, 2020

    Optimizing COVID-19 management through highly sensitive SARS-CoV-2 detection test. Luxembourg (Luxembourg), Metz (France) — May 21— Advanced Biological Laboratories (ABL) announced today the CE-IVD registration of its UltraGene® Combo2Screen SARS-CoV-2 assay, now available for in-vitro diagnostics u…

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  • Advanced Biological Laboratories Receives CE-IVD Registration for its SANGER and for its NGS DeepChek®-HIV Genotyping Drug Resistance Assays

    May 18, 2020

    A unique and flexible solution adapted to all virology and microbiology laboratories   LUXEMBOURG CITY (Luxembourg), METZ (France) — May 18th, 2020 — Advanced Biological Laboratories (ABL) announced today the CE-IVD marking of its DeepChek®-HIV assays, now available for in-vitro diagnostics.  Intend…

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  • UltraGene Combo2Screen SARS-CoV-2 Assay Now Supported by French ANSM

    May 13, 2020

    Luxembourg (Luxembourg), Metz (France), Boston (USA) — May 13 — Advanced Biological Laboratories (ABL) announced today that its RT-PCR test for COVID-19 detection UltraGene® Combo2Screen SARS-CoV-2 assay is now officially approved by the French ANSM (Agence nationale de sécurité du médicament) as a…

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