Process Capability :   One pilot factory and three manufacturing factories with seven multi-functioned production lines, equipped with more than one hundred of reactors in material of glass-lined, carbon steel and stainless steel, as well as full set of transforming facility of biological enzyme catalysis. Capacity of reactors covers the range from 50-500L (in pilot factory) and 1000-6300L (in manufacturing factories), guarantees production from grade of kilogram to tonnages of commercial manufacture. · Completed regular synthetic units and chemical engineering units including extraction, dropping, distillation, rectification, filtering, drying and refined-finishing areas.

After-sale Service :   GMP regulation is followed in the daily management. Quality department is responsible for the quality control of the total manufacturing process and quality management, maintaining the persistent improvement of product quality to meet the requirement of the customers. A three-level quality supervision network is established to ensure the execution of quality management in the company. A system of rewards and penalties strengths the responsibility of all employees. QA system has accepted the audits of decades of pharmaceutical companies from the world. The documents concerning the registration of products in EMA, PMDA and FDA are supplied for the approval of the drugs.