Research On The Construction Of Chinese Defective Drugs Management System

In recent years,China's defective drugs caused serious damage incident frequently,threatening public health and safety.As a result of the current management of defective drugs in our country only focusing on drugs of inferior quality and fake drugs,with the result that some drugs are still on sale in the market, which may be in line with the relevant standards,however there is a risk to public health in these drugs.These drugs mentioned above are the unnecessary risks to the public.Based on the background above,the paper is designed to establish a framework of defective drugs management system which suits to China's situation.First,this paper adopt the literature research method to finish the review of research on defective product and defective drugs.Then,the paper stated regulation theory and main laws and regulations involved defective drugs,which are foundations of this paper.After that,make reference the concept of defective products from abroad and combined with the special nature of drugs,the paper introduced the definition of defective drugs,and classified.Then,the paper stated the current situation of the management of defective drugs in China.And it analyzed the problem in existence.Aiming at these problems,this paper described defective drugs management system of Britain and the United States and did a systematic study on social regulation supervisor and the defective drugs management system in these two countries including defective drugs report collection,early evaluation,investigation and information service system,and then draws some helpful inspirations in constructing a defective drugs system. On this basis,the paper put forward strategies on how to establish a defective drugs system.Firstly,establishing a perfect defective drugs legal system,providing a stable guarantee;secondly,putting forward the choice of setting up a sound organizational system.Thirdly,establishing defective drugs management system including a defective drugs report collection system,a early evaluation,investigation, a scientific defective drugs evaluation system,appropriate measures to choose and a defective drugs information issue system and so on.