Founded in July 1969, the company, formerly known as Jiangxi Lianhua pharmaceutical factory, is located in Lianhua County, Jinggangshan old revolutionary base. In July 2000, it was restructured and established into a new private company through investment promotion. It is a key business enterprise in Pingxiang City. It is a manufacturer of API, Chinese patent medicine and pharmaceutical intermediates, and has fully passed the national GMP certification. The company's quality management system is directly under the leadership of the general manager, with quality management department, QA and QC. Perform the functions of quality supervision, management and quality inspection respectively. The quality management department is responsible for establishing and improving 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 material procurement, warehousing acceptance, production process, finished product release, sales and customer feedback, and standardize and improve various quality management systems; At the same time, manage the whole quality system of the company through on-site patrol inspection, regular inspection and regular quality report, and regularly organize GMP knowledge update training to improve the quality concept of all employees. The central laboratory (QC) is responsible for the inspection of raw and auxiliary materials, finished products, intermediates and process water used in the company's production and the monitoring of environmental conditions. Jiangxi Dadi Pharmaceutical Co., Ltd. is headquartered in Lianhua County Industrial Park, Pingxiang City, Jiangxi Province. It has production bases in Pingxiang, Jiangxi Province and Yancheng, Jiangsu Province, covering a total area of nearly 400 mu, with total assets of more than 250 million yuan. The company is mainly engaged in raw materials and intermediates such as levofloxacin hydrochloride, levofloxacin lactate, ciprofloxacin hydrochloride and simvastatin, various dosage forms of Chinese patent medicines, chemical raw materials and products. It has a number of drug number approvals. The raw materials products have fully passed the national GMP certification, and the products are sold to all parts of the motherland, Europe, America, India and other countries and regions. The company adheres to the corporate purpose of "reporting the earth with hard work and contributing to mankind with health", carries forward the corporate culture of "love and dedication, customer first, honesty and trustworthiness, and win-win cooperation", is committed to developing the national pharmaceutical industry, strengthening enterprise standardized management, and providing customers with better products and services.