Grassroots Level Supervision Existence Of Our Country And Drug Problems And Countermeasures

2006 Qi II drugs, such as counterfeitXinFu, the melamine case in 2008, has always put the little-known food and drug regulatory authorities to the wave above the tuyere.Drugs because of the relationship between the people's lives and health are a special commodity, so the countries of the drugs are strict government supervision to ensure that the people use safe and effective.With the reform of China's pharmaceutical and medical security system to promote and set up a socialist market economy, the pharmaceutical market became more complex, diversified, illegal drugs, medicines a direct threat to people's lives and health, drugs become a majority of the people most concerned about hot spots , the focus of difficult problems.In 1998, a significant streamlining of government agencies, the Central Committee and State Council decided to set up the National Drug Administration, and the formation of the country's pharmaceutical supervision and management system. Practice shows that over the past few years, China's Drug Administration job indeed made unprecedented progress, the initial solution to the drug supervision and administration and the pharmaceutical industry manage the contradictions and solve the industry's internal struggle permissions. But not yet thoroughly does the discussion and the research have to carry on the rules and regulations in these aspects, how the rules and regulations, as well as who carries out questions and so on rules and regulations, in reality the goal and the direction are not often clear about, the method and the measure are ineffectual, obtains with difficulty should have, a better effect. Therefore, urgent needs further to study our country drugs management system question, strengthens the drugs the management by supervision, safeguards people's medication security.This paper first introduces the basic theory and Drug Administration regulation of China's pharmaceutical development process, followed by combination of the author's own actual drugs found in the grass roots of our regulatory problems: first drug lack of human resources; Second pharmaceutical laws and regulations are not perfect; third masses of the people inadequate understanding of drug regulation; fourth regulatory unclear division of responsibility.And analysis of grassroots drugs supervision and the cause of the problem exist: first started late, has not placed enough emphasis; second from abroad, one-step too-span; third system is not perfect, and regulations are not perfect.Finally, the Perfection of the grass-roots response to drug administration: first to strengthen self-construction of Drug Department; second regulatory change, enhance regulatory efficiency; third perfect laws and regulations, efforts to increase law popularization; fourth drugs and give full play to the "two net" effect; fifth perfect Drug ads regulatory mechanism.Strive to further strengthen the pharmaceutical supervision and management, to promote the people's diet drug safety a contribution to make.