AusDiagnostics inc., Roche Diagnostics Inc., Vivacheck Inc., Zhijiang Group LTD., CTK Group LTD. (TGA) and Hollogier Group Inc. (TGA) on Saturday, March 22, according to the Australian Drug Administration (TGA). Hangzhou Otai, Vivacheck and Shanghai Zhijiang are domestic IVD enterprises.
In the United States, according to the official website of THE FDA, the real-time fluorescent RT-PCR kit produced by BGI for the detection of SARS-2019-NCOV has been approved by the FDA and can be officially put into the epidemic prevention and control in the United States. This is the first Chinese product that has passed the FDA’s emergency authorization.
In fact, Chinese IVD enterprises have the ability to go abroad and compete with world-class enterprises.
Hangzhou Realytech has passed THE FDA certification. The novel Coronavirus detection rate is high. Please feel free to contact us if you need to purchase a coronavirus quick detection reagent in large quantities.
Post time: May-27-2022