❆ Isiqinisekiso senkqubo ye-EU TUV ISO13485 kunye nomzi mveliso oqinisekisiweyo we-USA FDA;
❆ Ngaphezu kwama-30 izatifikethi zobhaliso lwezixhobo zonyango ze-NMPA eTshayina;
❆ I-Novel Coronavirus Test Kit iye yaqinisekiswa yi-US FDA EUA, EU CE, French ANSM, Netherlands, Germany BfArM, Austria, Australia TGA, Brazil ANVISA, Bolivia, Peru, Thailand, Philippines, Indonesia, Malaysia kunye nezinye iziphathamandla zehlabathi kunye zidweliswe kuluhlu olumhlophe lwabarhwebi abavela kumazwe angaphandle, okwangoku ubhaliso e-China i-NMPA, i-WHO kunye nolunye ubhaliso oluhambelanayo luyaqhubeka.
![01](https://cdn.bluenginer.com/WkPp1DSzQ3P6NZ5P/upload/image/20231121/acf11888b8cc320229c91a3e509b1706.jpg)
![36](https://cdn.bluenginer.com/WkPp1DSzQ3P6NZ5P/upload/image/20231121/25e14f67b21d3e1c44508fb4da892058.jpg)
❆ Ibhetshi yokuqala yenoveli yaseJamani i-coronavirus self-uvavanyo iimveliso zifakwe kuluhlu lwe-BfArM lwamashishini.
❆ Iimveliso zovavanyo lweziyobisi zidweliswe kwi-"Ministry of Public Security Ikhithi yoVavanyo lweZiyobisi (imigca) ekucetyiswa ukuba iThengwe iKhatalogu”;
❆ ILaihe Biotech iphanda kwaye iphuhlise ngokuzimeleyo “iQuantum Dot Fluorescence - iqonga lokuyila lobuchwepheshe lokuFumana iziyobisi ngokuKhawuleza kweNwele” elifana neprojekthi “ye-13 ye-5-Yeminyaka” yesizwe engundoqo ye-R&D, njengeyunithi yentsebenziswano yoshishino ekubhaqweni kweziyobisi kunye nolawulo gwenxa lweziyobisi kunye neprojekthi yophando lwezixhobo isihloko iziphumo ezi-5 zophando;
❆ Ilungelo elilodwa lomenzi wechiza elifunyenweyo: ngaphezu kwe-30 yamalungelo awodwa omenzi wechiza kumazwe ngamazwe nawaseTshayina.