With The Drug Supply Chain Management System Design Of Pharmaceutical Distribution Enterprises Based On GSP

Pharmaceutical industry, as the fundamental of livelihood in modern society, is becoming increasingly important. Medicine management is becoming the most important part in the pharmaceutical industry. Especially in the drug marketing and distribution process, continuous supervision of the quality of drugs is becoming the main difficulty in drug administration. To protect the health of the people and the safety of drug effectively, since 2004, the Chinese government implemented a mandatory drug quality management specification for pharmaceutical enterprises, GSP scilicet. Although the development of computers has been widely used in pharmaceutical companies, but the current management information systems and GSP management system are not getting organic combination. The traditional medical management information system has import, sale, store,financial and other modules as the core modules, but does not pay much attention to pharmaceutical quality control, while the quality of drugs is directly related to the health of millions of patients. The pharmaceutical management system based on the drug quality needs to be established in urgent.This paper designed and implemented a medical management information system based on GSP. The study first describes the current situation of medical management information system based on GSP at home and abroad, discusses the main design architecture involved in systems- C / S and B / S architecture and their related development technologies, and establish a technology system that suit for universal demands via comparing the advantages and disadvantages of related technologies. Second, combine the system with the status of pharmaceutical firms, and do field researches with the sample firms, discuss the demands with its industry characteristics, analyze the medical management system requirements, such as custom situation, business processes and system functions; Then, design the system and database with their industry characteristics requirements. Finally, the performance test, reliability test and compatibility test prove that the system is easy to operate. Meanwhile the system is stable and reliable, it also has rigorous design logic and good compatibility. It is accepted by the pharmaceutical industry with its effectiveness, convenience, quickness and the cost of deployment, reached the expected study design goals.