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Are AnteoTech (ASX:ADO) rapid COVID tests available in Australia?

AnteoTech (ASX: ADO) stock has soared on the development of its COVID-19 rapid antigen test, but the 15-minute test still hasn't received TGA approval. ....

United States , Western Australia , Derek Thomson , Anteotech Eugeni , Annastacia Palaszczuk , Anteotech Ltd , Therapeutic Goods Administration , Courier Mail , Queensland Premier Annastacia Palaszczuk ,

Local made rapid COVID test launches in EU, seeks Australian approval


Local made rapid COVID test launches in EU, seeks Australian approval
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Crowds at airports, sporting matches and music concerts overseas could be screened for COVID-19 using a new rapid test developed by a Brisbane biotech company.
The test could form a key plank of the ongoing recovery from the pandemic after securing approvals in Europe and the UK but any Australian rollout may not come until next year at the earliest.
Tek Shen Ling (left) one of the head developers of AnteoTech’s EuGeni rapid covid tests, with Deputy Premier Steven Miles. ....

Derek Thomson , Anteotech Eugeni , Premier Steven Miles , டெரெக் தாம்சன் , ப்ரிமியர் ஸ்டீவன் மைல்கள் ,

AnteoTech officially launches 15-minute rapid COVID-19 test


Date Time
AnteoTech officially launches 15-minute rapid COVID-19 test
Deputy Premier and Minister for State Development, Infrastructure, Local Government and Planning The Honourable Dr Steven Miles
Queensland company AnteoTech has officially launched its 15-minute COVID-19 antigen rapid test (ART) platform, EuGeni.
Deputy-Premier and Minister for State Development Steven Miles joined the official global launch today in Brisbane.
“It has been a great period for AnteoTech, which recently gained the health and safety approvals to sell this technology in Europe and the United Kingdom,” Mr Miles said.
“We are proud to have assisted in making this moment a reality.
“The Palaszczuk Government committed $1.4 million through the Essential Goods and Supply Chain Program to help AnteoTech to progress the EuGeni platform and COVID-19 ART from prototype through to product launch.” ....

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AnteoTech Secures CE Mark for Its Versatile EuGeniTM Rapid Diagnostic Platform


Apr 26 2021 Read 16 Times
AnteoTech’s EuGeni™ Reader and high-sensitivity COVID-19 Antigen Rapid Test (ART) have received Conformité Européene (CE) Mark registration as the company looks to progress with European distribution. A saliva-based COVID-19 rapid test is also being validated for the platform. The digital multi-test EuGeni Reader eliminates human error associated with current lateral flow test interpretation, and can support high-sensitivity quantitative readouts for time-critical disease and clinical intervention tracking. The COVID-19 ART boasts exceptional sensitivity and specificity, and delivers test results in less than 15 minutes. As such, it will be a key tool to support efficient front-line screening as economies look to reopen across the continent. The first-of-its-kind, ultra-high-sensitivity COVID-19 saliva test currently being developed for the EuGeni Reader overcomes the poor sensitivity of currently available saliva-based COVID-19 tests. ....

Derek Thomson , Anteotech Eugeni , Laboratory Information Management Systems , Rapid Test , Eugeni Reader , Eugeni Platform , Chief Executive Officer , Co Vid , டெரெக் தாம்சன் , ஆய்வகம் தகவல் மேலாண்மை அமைப்புகள் , விரைவான சோதனை , தலைமை நிர்வாகி அதிகாரி , இணை வித் ,