Quality system of Jiangsu Zhongbang Pharmaceutical Co., Ltd.

The company's quality management system is directly led by the general manager, with a central laboratory and a quality management department. Exercise the functions of quality inspection, quality supervision and management respectively. The central laboratory is responsible for the inspection of raw materials, intermediates, health products and process water used in the company's production and the monitoring of environmental conditions. The quality management department is responsible for establishing and perfecting the company's quality supervision system, and has set up full-time QA personnel to monitor the whole process of material supplier evaluation, raw and auxiliary materials procurement, warehousing acceptance, production process, finished product release, sales and customer feedback, and standardize and improve various quality management systems; At the same time, through on-site inspection tour, regular inspection, regular quality report and other ways to manage the company's entire quality system, organize regular GMP knowledge update training, and improve the quality concept of all employees. In 2003, the company began to implement the ISO9000 quality management system and passed the ISO9000 quality system certification. In 2004, GMP management was gradually implemented and passed the national GMP certification for the first time in the same year. In the past 9 years, the company has been certified by domestic GMP for 3 times and has been audited by domestic and foreign customers for many times. So far, all products approved by the company have passed GMP certification. The company plans to pass the double GMP certification in Europe and America around 20 13-20 14.