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Audere Gets FDA Emergency Use Authorization for SARS-CoV-2 At-Home Sample Collection Kit

Industry news | 06 December, 2021 | CACLP

Original from: Genomeweb


The US Food and Drug Administration on Tuesday granted Emergency Use Authorization for an at-home sample collection kit for SARS-CoV-2 molecular testing developed by nonprofit digital health firm Audere.


The HealthPulse@home kit is designed for the self-collection of anterior nasal swab specimens by individuals aged 16 and older, as well as the collection of samples by adults in individuals aged 2 and older. Samples can be transported at ambient temperatures for in vitro diagnostic SARS-CoV-2 RNA testing.


Testing of HealthPlus@home samples is limited to Audere-designated labs that are CLIA-certified to perform high-complexity tests, according to the FDA.


In addition to the sample collection kit, Seattle-based Audere has developed a COVID-19 symptom tracking and surveillance tool that is currently used by a local fire department.


Source: Audere Gets FDA Emergency Use Authorization for SARS-CoV-2 At-Home Sample Collection Kit

Filed under:
FDA
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