The Research On Issues And Countermeasures Of Drug Registration In China

Drugs are used for prevention, treatment and diagnosis of diseases, regulatinghuman physiological function and provides indications or functions, usage and dosage,including Chinese herbal medicine, Chinese Herbal Medicine, medicine, chemical theirpreparations, antibiotics, biochemical drugs, radioactive pharmaceuticals, serum,vaccines, blood products and diagnostic medicines. Implementation of effectiveregulatory relationship of pharmaceutical drug safety to consumers related to themaintenance and protection of the rights and interests of the public life and health. TheChinese government always attached great importance to the Drug Safety Regulation.Over the years，in order to strengthen the Drug Safety Regulation and safeguard thepublic’s medication safety, the government gradually established and improved DrugSafety Regulation and management system.Constantly improved the Drug Supplysystem, improving the quality of medicines. Maintained the public rights of drug using,and strive to improve the health level of the public. Drug safety issues have become themajor issues that related to the state image and credibility. However, in recent yearsdrug safety issue events have occurred continually, which reflects that we still existsvery serious drug regulation issues.To strengthen then the drug registration stage, followed questions, analyzeproblems, the general argumentation method to solve problems. According to thehundreds of years history of the United States Food and Drug Administrationdevelopment, summed up available suggestions for our government Drug Regulatory Authorities. As well as a comparative analysis, giving some solutions from the othercountries’ advanced experiments.This paper studies the content is divided into five chapters. Overview the recentresearch and the introduce this study’s background. The second chapter is mainlyexplained the drug regulatory department responsibilities and some basic principledefinitions of the drug regulatory issues. Chapter Ⅲ is focused on analyzing the exitsissues of drug registration regulation and the causes of the problems. Chapter Ⅳ andⅤare the focus of this article. Introduction the century-old history of the United StatesFood and Drug Administration, and learning some new strategies from it advancedexperiments. Author gave three suggestions to improve the existing Drag RegulationSystem and hopefully that will effectively increase the government regulation powerand ensure the public medicines safely.