Government Regulation In Drug Safety Crisis

The drug quality have a very important bearing on the human health,the qualified medicines can provide the health protection,while counterfeit and substandard medicines pose a direct risk.As a result of pursuing interests in the production,some domestic drug manufacturing enterprises regardless of morality and responsibility and harm civil lawful healthy rights.As a regulator,government should provide production for citizens if market regulation failed.So it is the chief task for our supervisory and management organ to improve the systems and measures,strengthen drug regulatory capacities through using the experience of the advanced experience at home and abroad,they should solve the problems under the current supervision management by using rational organization and effective regulatory tools.The Changchun Problem Vaccine Event,in addition to the enterprise's own violations of the law and regulations,ignoring the moral bottom line and other issues,but also exposed the inadequacies of the government as a regulator in the work.This article reviews and analyses the whole process of Changchun Problem Vaccine Incident,and separately analyses the whole process of government supervision in the problematic event.Find out the key points of the problem incident,and the crux of the government's inadequate supervision in the whole incident.According to the exposed problems,the causes are analyzed,including the unreasonable existing supervision system,the imperfect supervision mode,the insufficient supervision manpower and the improvement of comprehensive quality,the punishment and the poor communication of information.Comparing the existing experience of drug regulation in the United States,combined with the actual situation of our country,the paper summarizes the corresponding countermeasures and suggestions,hoping to provide help for the government to improve the regulatory system,enhance the regulatory capacity and make up for regulatory loopholes.In 2018,with the completion of the reform of state institutions,China Food and Drug Administration was merged into the State Administration of Market Supervision.The comprehensive law enforcement ability of the supervisory team has been improved,and the supervisory ability has also been improved.The former decentralized supervision of various departments has been transformed into a unified centralized supervision,which is conducive to improving the efficiency of supervision and reducing the cost of supervision.It has great benefits for realizing the function of market supervision,maintaining the order of socialist market economy,protecting the rights and interests of the common people from infringement,and cracking down on illegal and illegal phenomena such as fraud and fraud.