Study On Drug Supervision Informationization Based On The Construction Of E-government Information Platform

Drugs are a special commodity,which is closely related to people's physical health and life safety,thus supervision of drug safety is particular important.The current mode of drug control is relatively mature in our country,which could effectively maintain the rational order of the drug market,and severely crack down on illegal activities in the areas of drug production,operations,and use.However,in recent years,the situation of drug safety in our country is still not optimistic.Drug safety incidents such as “Chromium capsules” and “vaccination incidents” have occurred repeatedly,which has severely disturbed the order of the pharmaceutical market and violated the legitimate rights and interests of the people.All these problems suggested that the work on drug safety supervision still needs to be improved.With the development of society,traditional drug regulatory models have failed to meet the current and future demand for drug safety supervision.The reform of drug regulatory models is imperative.Based on drug regulatory laws and regulations and e-government theories,herein,we start with the actual processes and needs of drug supervision to further analyze the drug Information supervision and construction by using literature analysis methods,research and analysis methods,questionnaires,and comparative analysis methods.The first chapter of this article briefly outlines the background,purpose,and significance of the research,and detailedly introduces the ideas,contents,and research methods.The second chapter introduces the concepts and theoretical foundations related to pharmaceutical information regulation and analyzes the necessity and feasibility of drug information construction;The third chapter introduces the development status of China's traditional drug supervision methods and informationization supervision construction,and puts forward the existing problems.The fourth chapter analyzes the literature to understand the basic situation of pharmaceutical informationization supervision in developed countries,and sums up lessons for reference.Chapter 5 gives a brief description of the status and existing problems in the supervision and management of drug informationization in Tianjin;The sixth chapter puts forward specific proposals for the development of supervision of drug informationization.This research has made innovations on the basis of current research.First,it focuses on the construction of an integrated and integrated platform,and strives to achieve the "one-stop" regulatory goal.The second is to focus on multi-role participation in the regulatory process to meet the needs of different participants;The third is to focus on the expansion of regulatory measures,and realize the three-dimensional supervision of drug safety through video,voice-activated,location-based navigation and other technical means.