China will raise the pharmaceutical industry admittance threshold

Recently, the state council issued the "national drug safety" 1025 "plan". In the drug safety protection, "planning" points out, "1025" period, countries will improve medicine industry admittance threshold, establish the credit archives from personnel of serious violations and the enterprise and employees promise of banned industry and promote the pharmacists method for practice, strengthen the practice medicine guru equipped with use dynamics. "Planning" should be made to improve security and drug safety supporting NFL Hats policies. Perfect medicine industry policy, improve the admittance threshold, strictly control the number of new open enterprise guidance for enterprises, m&a, promote resource advantage to the enterprise central; Support biological medicine, medical equipment industry healthy and rapid development; We will vigorously support traditional Chinese medicine, national medicine development, promote the inheritance and innovation. Drug research and improve economic policy, to have reached the international level of generic discount sunglasses drugs, in drug pricing, public bidding, medical care and support to submit an expense account, form is helpful to improve the quality of drugs, security and drug safety incentive mechanism. Perfect strengthen drug safety science and technology policy, strengthen technology to drug safety support role. Creating new drugs such as carrying out important national science and technology major projects and the national science and technology plan, support and encourage enterprise technology innovation, improve the drugs, medical equipment in the innovation ability. To enterprise as the main body, the combination of production, to promote drug safety research work. The planning of the requirement to carry out the drug safety responsibility. According to the local government overall responsibility, supervision department, enterprise is the first person in moved to the requirements of ", further improve the drug safety responsibility system. Enterprise to earnestly implement the drug safety responsibility, perfect quality management system, strictly carrying out quality management standard, forbid not qualified factory, drug sales, timely recall problems drugs and retreat city drugs. Carry out enterprise credit rank evaluation work, establish the credit archives from personnel of serious violations and the enterprise and employees promise of industry allowed. Regulators want serious to perform supervisory duties, strengthen drug research, production, circulation, and use of the regulatory process, supervision and enterprise in strict accordance with the national laws and regulations and quality standard production, sales, drug adverse drug reaction monitoring and to the risk warning, and punishes the illegal behavior, ensure safe drug use. The local governments at various levels shall be responsible for the administrative divisions of the drug safety work, will be included in the government drug safety assessment assessment system, establish evaluation and the responsibility system. The regulator to sound levels and rural and drug network, make sure drug regulators to work independently in accordance with law. "Planning" should be made to improve drug safety laws and regulations. Promote practice method for the pharmacists, amend the pharmaceutical administration law of the People's Republic of China ". Revising "medical equipment supervision and management regulations", the management of radioactive drugs including measures of rules and regulations. To research and develop of prescription and non-prescription drugs classification management regulations. The planning of the specified, will improve practice medicine guru system. With the deepening medicine health system reform, and make the implementation of standard business practice pharmacists, practice strict pharmacist access, and promote the pharmacists continue to practice education project, improve the practice medicine guru overall quality, promote the pharmacists team development practice. Increase the practice medicine guru equipped with use dynamics, since 2012, the new launch retail pharmacy practice must be equipped with the pharmacists; To "1025" at the end, all retail enterprise legal persons or main managers must have the practice qualification pharmacists, all retail pharmacies and hospital pharmacy business practice medicine guru guidance is the rational use of drugs, exceed the time limit not reach the requirements, the cancel sales medicine qualification. The planning of the emphasis on, need to strengthen drug safety regulatory ability construction. Innovation and drug safety law enforcement system and mechanism, promoting the drug inspector of full-time staff construction. Enrich the country and province level two drug evaluation evaluation, check the authentication, monitoring and warning strength, make sure drug and evaluation, such as again register work smoothly. Deepen the reform of the system of administrative examination and approval drugs, strict examination and approval standards, standardize examination and approval procedures. Governments at all levels should will drug safety supervision funds into the financial budget, increase the funds investment. Strengthening primary, remote areas and minority areas drug safety ability construction, improve the basic law enforcement conditions. Strengthen and international organizations, foreign regulators and non-governmental institutions of the exchange and the cooperation, from the international advanced supervision experience, and constantly improve the regulation ability and level. "Planning" and points out that the implementation of plans to strengthen the organization leadership. Local governments at all levels should according to this plan definite development goals and the main tasks of drug safety work into the important agenda and regional planning for social and economic development. All departments concerned should according to their respective functions and duties, targets, task decomposition, formulate concrete implementation plan, to the implementation of the related tasks. And in the middle of 2013 by the end of 2015, the food and drug administration lead to plan with interim assessment and eventually period of evaluation, evaluation and assessment results to the state department report.
see more:Why the French never but the June 1 children's day?
Why the United States rarely make waste electricity