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  Zhongxin pharmaceutical quality department is mainly responsible for the quality management and inspection of the whole process of the company's product development and production. The team of quality department is composed of high-quality and experienced professionals. With solid professional knowledge, rich working experience, quality system established and implemented in strict accordance with GLP, GMP and ISO standards, as well as advanced inspection and analysis instruments, they closely monitor all the processes of R & D and production, eliminate quality problems in all links, and ensure "high standard, standardization and zero defect" of achievements and products.

  research and development

  "Quality control, safety and effectiveness" is an important principle in the process of drug research and development.

  Quality comes from design. The quality management in the process of drug research and development is the initial activity to control product quality, and its quality management level determines the drug quality. Excellent quality management can effectively save money, speed up the research and development process, and improve the overall efficiency. According to the standards of GLP and ISO, the quality department of China New Zealand medicine has established a strict quality system, and organized research and experiments based on the drug management law, drug registration management measures, GLP and relevant laws and regulations.

  production

  According to the company's objectives and tasks, from the general manager, quality department to production departments, the responsibility should be assigned to each person, and each process in each link should be checked at all levels. The three-dimensional and all-round monitoring should be carried out on material purchase, warehousing, material picking, production process, intermediate product inspection, internal and external packaging, finished product inspection and re inspection, so as to ensure that the products are "safe, effective, uniform and controllable". The quality department also specially checks and tests the key links to ensure that the environment, process and products are in a standard state. If the production is not in accordance with the operating procedures, the responsibility will be investigated, and unqualified products will never be allowed to go out.

  Two members of the quality department team have obtained YY / T0287-2003 quality management system standard internal auditor qualification certificate.

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Address: Building 7, Kangyuan medical science and Technology Park, 578 longmian Avenue, Jiangning District, Nanjing City, Jiangsu Province
Postal Code: 211100
Contact information: 025-58310595 (switchboard)
Fax: 025-58310595-108

 

江苏中新医药有限公司

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