2012年4月5日星期四

Jia qinglin met with king Cambodia

President of CPPCC jia qinglin 13 in the diaoyutai state guesthouse, met with king Cambodia west confit. Jia qinglin first conveyed the President hu jintao cordial greetings and good wishes. He said that in your majesty and west sihanouk intervened continuously, his majesty's concern confit, after the two countries to the joint efforts of the government and the people, of Cambodia comprehensive strategic partnership continuously consolidated and developed. Jia said the two countries of Cambodia high-level exchanges, places and folk communication is very active, each field friendly practical cooperation fruitful, for the two peoples real benefits. Jia said that, the Chinese side will continue to support Cambodia go accordant with the development way, and support economic development, Cambodia improvement of people's life. Potential economic and trade cooperation of Cambodia, the Chinese side will take active measures, to expand the imported from Cambodia, to encourage strong, reputable Boston Bruins Snapback enterprise investment to Cambodia, encourage more Chinese tourists traveling to Cambodia, support the two countries to strengthen the friendly exchanges and cooperation in place. Jia said that believe in Cambodia royal concern, in the two governments and people's joint effort, of Cambodia friendly relationship will constantly radiate new Cheap sunglasses vitality. West, please convey to monitor jia qinglin, President hu jintao cordial greetings and good wishes. West ha monitor said, Cambodia peoples have affection to each other. The Cambodian government and people's heartfelt thanks to the Chinese government and people for a long time to Cambodia's selfless support and help. Highly JianFang China in various fields of development achievements obtained, with the Chinese side to work hand in hand to promote in Cambodia and friendly cooperation relationship to get consolidated and developed. West, JianFang reiterated that the firm will continue to monitor the one-china policy.
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Beijing will match professional guidance for worker employment

Recently on the introduction of the "Beijing" 1025 "period worker development planning" proposes that in the year 2015, professional, qualified, full-time employment guidance and guiding teacher and the proportion of the number of staff and workers to achieve at 1:30, employment and guidance for the proportion of the zone maps.map division to. Reporters 13 from the Beijing municipal federation of trade unions that promote labor standards and harmonious relationship, it is still the "1025" period of Beijing worker is the key point of the development. The aim is to increase their employment ability and quality, help them realize the stable employment. According to introducing, Beijing will from professional human resource service agencies of the employment guidance and counselling staff improve the degree of specialization, especially the social organization of Boston Bruins Fitted Hat such persons specialized level, in order to improve the government and the society to the special ability employment promotion career. At the same time, Beijing will be to community service, government agencies and the intermediary organization and so on employment and guidance personnel of personnel standardization authentication, in order to regulate the Discount sunglasses practice qualification, thus improving the organization of of all kinds of employment promotion service ability and service effect. It is reported, will the worker's right to employment, ShouRuQuan, safety, security, to participate and right of professional development as a measure of the realization of the development status of the rights of the important index, Beijing is "1025" worker development planning is the important component of the trade union in the system also belongs to the initiative.
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2012年4月4日星期三

China's drug safety conditions improved obviously

Recently, the state council issued the "national drug safety" 1025 "plan". The planning of the points out, "eleventh five-year plan" period, China formed a complete set of pharmaceutical production and supply system, a basic covers drugs development, production, circulation and use the security of the whole process of the supervision system, drug safety status markedly improved, and drug safety guarantee ability obviously improved. The planning of the first introduced the current situation of drug safety, and points out that the "eleventh five-year plan" period, drug safety conditions improved obviously. The national drug evaluation total sample rate significantly increased, chemicals, medicine, biological products market rate of increase in drug quality on the whole maintained good level. "The drugs register management method" after the enforcement of this amended in 2007, and to promote the registered approval standards, strict pharmaceutical production access, and new listed generics quality improved obviously. Adverse drug reaction monitoring, special drug abuse monitoring network warning effect is strengthening, and the drug safety emergency disposal capacity increases, gradually reduce drug safety events. At the same time, the public use basic meet demand. Implement the national basic drugs system, ensure the cheap new era hats basic drugs rights and interests. Creating new drugs ability raise further, drug logistics system, building steadily, and the drug supply covering both urban and rural basic network is built, the public daily medicine basic get satisfy demand. Set up the national drug reserve system, improve the response to major outbreak of disasters drug support capacity. The "eleventh five-year plan" period, China's drug safety regulatory ability also increase. Establish a more complete national, provincial, city and county level administrative supervision system, building on wholesale nfl jerseys the drug registration evaluation, standards, the examination, adverse reaction monitoring for the key technical support system, improve the with the pharmaceutical administration law of the People's Republic of China "and" the medical equipment supervision and management regulation "as the core system of laws and regulations, formed the pharmacopoeia of the People's Republic as the core of the national drug standard management system. Further to improve the drug quality management standard, strengthening the drug regulatory process. Drug regulatory information construction has made some progress, special electronic supervision of the drug is progressing smoothly. Drug regulatory infrastructure improved obviously, significantly improve the quality of the team.
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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.
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