INDICAID(R) COVID-19 rapid antigen test is certified by the Cambodian Ministry of Health for Disease Control

Hong Kong and Phnom Penh, Cambodia, June 22, 2021/PRNewswire/ – The Cambodian Ministry of Health has approved the commercialization of the INDICAID® COVID-19 rapid antigen test as part of the country’s efforts to control the recent surge in COVID-19 cases .
The Cambodian government has deployed rapid antigen tests such as INDICAID® to carry out large-scale screening in the capital Phnom Penh and surrounding areas, using the short time and convenience of test results to help the government quickly identify COVID-19 patients and curb the spread of the disease. These tests also led to better containment measures, effectively dividing the capital into red, orange, and yellow areas based on the number of cases and the risk of transmission. INDICAID® can also be retailed in Phnom Penh.
Ricky Chiu, founder and CEO of PHASE Scientific, said: “We believe that the accuracy, ease of use and affordability of our test kits will make INDICAID® play an important role in the screening work carried out by the Cambodian government in the region. Role.” Official manufacturer of the INDICAID® test kit. “We welcome the decision of the Cambodian government and look forward to using our rapid test kits to support its neighboring countries.”
Chiu stated that many countries have adopted INDICAID® to combat COVID-19. In Hong Kong where PHASE Scientific is headquartered, INDICAID® has been recognized by the government as a designated product for hospital and nursing home visits. It is the best-selling brand among similar products and has sold more than 2 million kits. It is also widely adopted by hospitals, government and private companies, supermarkets, hotels and schools for regular local and international screening.
INDICAID® COVID-19 Rapid Antigen Test is a CE-labeled lateral flow immunoassay designed to qualitatively detect SARS-CoV-2 antigen in direct nasal swab samples. With reliable product quality and ease of use, INDICAID® can quickly provide results within 20 minutes, without the need for special equipment or facilities. The accuracy of this test kit has been clinically verified in the world’s largest dual-track clinical trial, in which INDICAID® was tested against PCR in more than 9,200 samples and showed high sensitivity and specificity.
INDICAID® is currently available in 33 countries and is in the process of obtaining an emergency use authorization (EUA) from the U.S. Food and Drug Administration (FDA).
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Post time: Jun-23-2021