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[Asia Economy Reporter Chunhee Lee] PHC's COVID-19 rapid antigen test kit is entering the Australian market.


PHC announced on the 14th that its affiliate, PhiloSys, received approval from the Australian Therapeutic Goods Administration (TGA) to sell its COVID-19 rapid diagnostic product for self-testing.


The approved product, 'Gmate COVID-19 Ag,' uses a saliva-based diagnostic method, boasting a sensitivity of over 95% and management capabilities through an application (app). The saliva diagnostic method minimizes discomfort for the test subject compared to the conventional nasopharyngeal swab method, reduces the risk of infection, and allows the test subject to easily collect and verify the specimen without the assistance of medical professionals.



A PHC representative explained, "By obtaining approval in Australia, the product's performance and quality system have been recognized to the extent that regulatory procedures can be simplified when entering other countries."


This content was produced with the assistance of AI translation services.

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