Country for PR: Hong Kong
Contributor: PR Newswire Asia (Hong Kong)
Wednesday, August 11 2021 - 03:00
AsiaNet
INDICAID(TM) COVID-19 Rapid Antigen Test Receives Emergency Use Authorization From the U.S. Food and Drug Administration
HONG KONG and GARDEN GROVE, Calif., Aug. 11, 2021 /PRNewswire-AsiaNet/ --

PHASE Scientific International LTD(https://www.phasescientific.com/) (PHASE 
Scientific), today announced that its INDICAID™ COVID-19 Rapid Antigen Test 
(INDICAID) received Emergency Use Authorization (EUA) from the U.S. Food and 
Drug Administration (FDA) on July 29, 2021. The FDA authorized the test for 
professional use in point of care CLIA-waived settings in the U.S. for the 
qualitative detection of SARS-CoV-2 antigen. Anterior nasal swab specimens may 
be collected by a healthcare provider or self-collected under the supervision 
of a healthcare professional. In regions outside of the U.S., such as Hong 
Kong, the test is authorized as a consumer self-test.

INDICAID requires no special instrumentation and can be performed in 20 minutes 
with a gentle shallow nasal swabbing vs. the deeper penetration required by 
other tests. INDICAID is also one of the first rapid antigen tests to enable 
batch sample collection and testing at the point of care due to its unique 
sample collection vial which protects the sample throughout the collection and 
staging process. The design gives healthcare professionals the option of 
collecting a large number of samples concurrently and then quickly testing the 
individual samples in batches within a two-hour timeframe. To date, there are 
over two million kits sold across 30 countries worldwide.

"Our test has been globally adopted and utilized to meet a variety of emergency 
testing needs. From the Hong Kong government using INDICAID for healthcare 
worker's weekly screenings to usage across shopping malls, supermarkets and 
schools worldwide, our rapid test has proved to be both effective and 
efficient," said Dr. Ricky Chiu, founder and chief executive officer of PHASE 
Scientific. "We see this U.S. emergency use authorization as recognition of the 
importance of our technology and product quality and we are eager to further 
expand our reach into more markets to do our part in helping combat the 
COVID-19 pandemic." 

About Phase Scientific International LTD: PHASE Scientific is a high-growth 
biotech company founded by a team of bioengineers from UCLA. The organization 
is focused on building tools that empower people by giving them better 
information about their health. Headquartered in Hong Kong, its footprint 
includes research and development, manufacturing and distribution in Hong Kong, 
mainland China and Southern California. For more information: 
https://phasescientific.com/. 

SOURCE:  PHASE Scientific

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   Caption: PHASE Scientific’s INDICAID COVID-19 Rapid Antigen Test has 
received FDA’s Emergency Use Authorization

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