Online Monitoring System For Medical Devices Under The Urban And Rural Development Research

With the overall development of urban and rural construction tasks of the advance, the traditional regulatory model for medical devices brings new challenges. With Internet infrastructure and information technology tools to change the way primary regulatory commission, to the maximum level degree of regulation of medical devices to play the advantages of information sharing has become an important issue. Use of network technology has matured, the use of advanced management information systems and software development platform, on-line monitoring for medical devices and scientific management, and supervision of cross-regional information sharing system boundaries to build an open, transparent regulatory information systems for medical devices, has been supervision of a medical device the best business model.For urban and rural development operations under the supervision of medical equipment online the characteristics of the Internet-based online monitoring system for medical devices development, aimed at regulators for the county commission, township supervisors, medical devices, providing a network-based information exchange platform, implementation of the system, structure of medical device manufacturers, enterprises, medical institutions, the use of personnel and medical equipment industry management of interaction between the bridge, promoting the sustainable development of medical device safety.This thesis studies the medical device regulatory status and trends, on-line monitoring of the purpose and significance of the urban and rural environment for the development of medical devices under the feasibility of building online monitoring system, pointing out that the use of networked information technology support tools to solve District Branch of the Department's monitoring commissioned by the process of township street problems, while using the Internet for medical equipment manufacturers, business units, medical device regulatory agencies focus on the flow of information in a timely manner the device reporting, adverse event information using the online management improve the efficiency of supervision; through the interaction of information between branches and the rapid exchange of regulatory activities by strengthening the arrangements and to assist the investigation.Then the system requirements analysis, systems development demonstrates the technical route and key technology selection, determine the overall system architecture, including the system's logical structure, functional structure, physical structure and user structure, the outline design description of each layer and design principles. The four subsystems of the system functional requirements and the modules described in detail to determine the system design principles, development environment, research methods, and the design of the main issues discussed.Finally, the pilot and test run through the system proved to propose the construction of the project objectives and requirements and meet future expansion requirements, while protecting the medical equipment production and business units of information security. System uses the j2ee architecture, database using ORACLE, used as a B-side JDBC data access technology. System realizes the operation and use of medical equipment production units, regulators and other interactive multi-network platform for the medical device regulators, entrusted with supervisory staff and production units to provide a quick and efficient and convenient information services.