The Design And Implementation Of Drug Comprehensive Supervision System Based On GSP Standard

GSP(Good Supply Practise)is the basis of thinking and understanding of drug supervision.China’s drug regulatory department is promoting the standardization and automation of the drug regulatory management system.On the basis of promoting the standardization of management,it can improve the efficiency and quality of drug supervision.At present,in some drug regulatory systems,there are problems such as poor service capability,insufficient information,and high regulatory operating costs,and it is difficult to truly reflect the core concept of GSP.Therefore,in order to solve the above problems,the development of a comprehensive drug supervision system based on the GSP standard is carried out.The drug comprehensive supervision system is based on the B/S architecture.The responsibilities of the browser and server components are defined to facilitate system maintenance in the B/S architecture.In the system development,the Hibernate+Spring Boot framework is applied.The Hibernate framework implements the whole process of transaction processing through the SessionFactory and Transcation components,and ensures system transparency on the basis of the application reflection mechanism.The Spring Boot framework takes the monitoring of business data as a basic feature and returns the monitoring results of tasks through the Pojo component.The application of the SQL Server database corresponds to the Spring Boot framework,ensuring data consistency based on monitoring data movements.The drug comprehensive supervision system has realized modules such as drug management,drug production management,supervision station management,knowledge base management,and system management.The drug management module realizes functions such as GSP sales management,GSP daily management,and integrity management.The pharmaceutical production management module realizes functions such as detailed product management,finished product report management,and daily management.The functions realized by the supervision station management module include account management,work report,supervision station assessment,and rural house banquet management.The knowledge base management module implements the variety information verification and the manufacturer’s record verification function.The system management module implements functions such as unit management,coordinating user management,user management of the unit,and user rights management.After the application of the system to the sound drug regulatory system,it will help improve the management quality and efficiency of the drug sales unit,and enhance the regulatory efficiency and service level of the regulatory department.It will effectively reduce the cost of drug supervision in the application of information forms,play the core concept of GSP standards,and ensure the standardization of drug regulatory management system.