Zhiyuan Biotech obtained its Drug Production License in 2013 and has since achieved certifications under ISO 9001 (Quality Management), ISO 14001:2015 (Environmental Management), and ISO 45001:2018 (Occupational Health and Safety). The company operates a GMP-compliant workshop covering over 2,000 square meters, supported by a comprehensive quality assurance system. Equipped with advanced analytical instruments such as Ion Chromatograph (IC), Capillary Electrophoresis (CE), High-Performance Liquid Chromatography (HPLC), and Fourier Transform Infrared Spectroscopy (FTIR), we ensure strict quality control and accelerate the development of new products.
A complete inspection procedure is in place to monitor all stages of the manufacturing process-from raw materials and intermediates to finished products. Additionally, we maintain a traceable system to identify inspection and testing status at every stage, guaranteeing compliance and consistent product quality.
