Research On Supervision Of Prescription Drug Sales In Retail Pharmacies

China implemented the prescription drug classification management system in 2000,the core of classification management is to strengthen the supervision of prescription drugs,to reduce the occurrence of unreasonable drug use,to ensure the safety of public drug use.However,in the past 19 years,how to effectively manage prescription drugs,especially the effective regulation of prescription drug sales in retail pharmacies has been a problem that remains unresolved.For that reason,many domestic experts and scholars have carried out a lot of research.they have put forward some valuable research results.But in reality,supervision of retail pharmacy prescription drug sales is still facing many pain points.Retail pharmacies illegal sales of prescription drugs has become an industry mess,in which the practice pharmacist "sell and affiliated certificate" situation is serious and form a black industrial chain.Faced with such a severe situation,government departments should take measures to strengthen supervision,in order to achieve the standardization of prescription drug sales in retail pharmacies,testing the wisdom and power of regulators.The problem is equally prominent in C district of Huizhou city.It has certain typicality.This thesis focuses on the difficulties faced by the regulation of prescription drug sales in retail pharmacies based on the sample of district C,takes literature analysis,field investigation,interview questionnaires and other ways to conduct in-depth research.On the basis of combing the research results of domestic and foreign experts and scholars,is based on the actual regulation of prescription drug sales in retail pharmacies in C district,and analyzes and summarizes the outstanding problems in the supervision.For the problem,multi-directional analysis,dig deep into the root cause of the problem.In order to explore the strategy of perfecting regulation,we comb edit the current situation and characteristics of prescription drug sales regulation in the United States,the United Kingdom and other developed countries,analyze the advantages of its supervision,and refine the enlightenment to us.Through systematic investigation and research,combined with the theory of market supervision and the theory of collaborative governance,the countermeasures and suggestions for perfecting supervision are put forward from five angles,such as policy system,laws and regulations,regulatory effectiveness,management measures and social co-management,so as to provide new ideas for promoting the scientificization of prescription drug market supervision,and thus enrich the drug market supervision theory.