The Company obtained the Medic-Device Production License in 2016, and operates in strict accordance with the ISO13485 quality management system. Through years of development, the Company has formed a complete industrialized system for the development, production and sales of in vitro diagnostic reagents and supporting instruments. The 15 existing products have obtained CFDA CE certifications, of these products, some have reached the international advanced level. We look forward to the clinical verification led by the World Health Organization and avoid application confusion caused by the quality difference of test kits. With multi-disciplinary integration as the means and core technology as the support, the Company provides the society with innovative products that are affordable, useful and worthwhile, and offers considerate health care services.