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The test measures the level of antibodies to the spike protein of the virus and can be used to establish immunity and vaccine efficacy.

The products combine next-generation sequencing and analysis with the company's NGSengine software to provide high-resolution HLA genotyping information.

The rapid chromatographic immunoassay detects SARS-CoV-2 using a nasopharyngeal swab and returns results in 15 minutes.

The tests measure patients' blood concentration levels of antipsychotic drugs to help psychiatrists manage their therapies.

The device also has Emergency Use Authorization from the US Food and Drug Administration and has CE marking for in vitro diagnostic use.

The IgG antibody test runs on the Architect i1000SR and i2000SR instruments and will expand to the company's Alinity i system.

Now, the assay can also be used with the Applied Biosystems 7500 Standard from Thermo Fisher Scientific, Roche's LightCycler 480, and Qiagen's Rotor-Gene Q.

Having recently won prequalification status from the World Health Organization the British Columbia-based firm is also considering US regulatory options.

The test could potentially enable labs to bring resistance testing in house, rather than send testing out to Canada's National Microbiology Laboratory.

The NEO Iris instrument uses the company's Capture solid phase technology for antibody screening and identification, and can run up to 60 tests and screens per hour.

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