As the most basic medical means, drugs can not only effectively treat and prevent diseases, but also directly affect the health of users. With the continuous improvement of the number and output of drugs, the quality and safety of drugs are the core tasks of pharmaceutical enterprises that can not be ignored. As an important means to detect the risk of problems, the effect of inspection and detection is affected by many factors, such as personnel, equipment, environment and so on. For this, major pharmaceutical manufacturing enterprises have the obligation to perform their duties and strengthen drug quality detection. In the context of the rapid development of science and technology, automation technology, information sharing platform, real-time monitoring system and so on have provided strong support for the development of drug inspection. Data integrity runs through the whole process of drug inspection. It is an internal demand and an inevitable trend to pay attention to the construction of drug research and development laboratory information management system (LIMS). Based on this, starting from the background of drug research and development stage, this paper explores the construction and design content of drug inspection LIMS, and puts forward corresponding construction strategies on how to improve the quality management level of drug research and development, in order to provide exchange and reference.

information management  /  drug inspection  /  management system