"Drugs factory

" Poison capsule "event once again sounded the alarm for the safety of drugs. Correction,abercrombie pas cher, Kinmen and Matsu, overseas, Xiu other well-known pharmaceutical companies have caught them, 13 products traced to possible carcinogenic chromium exceeded. Reporters found, drug quality supervision is not effective as people hoped, under the scrutiny of drug supervision departments, these chromium exceeded the capsule still openly on sale until the media exposure was only regulators found. All the way to the green light of chromium exceeded capsules, like a silent scream, issued a challenge to the existing drug quality monitoring system. Why release drugs listed companies held in their hands right Xiu Pharmaceutical is one of the largest pharmaceutical companies in Sichuan Province,abercrombie milano, 1,500 employees, annual tax capacity of about 50 million yuan. April 2011 due to drug quality problems have been investigated,abercrombie e fitch, to suspend business for six months. April 2012,hollister, the plant produced media exposure amoxicillin,hogan shoes, norfloxacin capsules measured chromium exceeded. Reporters learned that the Food and Drug Administration, Sichuan involved in the investigation, mothballed Xiu Pharmaceutical gelatin capsule material and suspended the production of hollow capsules,abercrombie sale, the media exposure products tested, the test results will depend on further treatment. Factory suspended sales of two drugs,hollester, but did not recall drugs. Both drugs belong to daily medication,hollister, combined with Xiu Pharmaceutical Pricing surprisingly cheap,holister, great sales in the country, the impact is extremely broad. Less than a year,goose jackets, twice the national quality shock events, Xiu Pharmaceutical pharmaceutical companies in the country can be described as the first loud. Drug regime here is how to execute it Guanghan City Secretary Food and Drug Administration Zhang Lu introduced, the council arranged two of Xiu Pharmaceutical unscheduled supervision, the key link for the production process, from the beginning of feeding, including whether the production process in accordance with the prescription. The core issue is, pharmaceuticals factory listing, release the power in the hands of the enterprise itself. Reporters asked: "Drugs factory, and the Food and Drug Administration regulation if there is no causal link must be agreed by the Food and Drug Administration to sign " Zhang Lu explicitly denied: "This regulatory requirements and everyday there are differences, not to say that every business batches of drugs shipped through the pharmaceutical sector must sign papers agreed to release. "reporter access to" Drug Administration Law of the People's Republic, "the second chapter of pharmaceutical production enterprise management, including the provisions of Article XII" Drug manufacturers must produce their medicines quality inspection do not meet national standards for pharmaceuticals or not in accordance with Chinese Herbal Medicine provinces, autonomous regions and municipalities drug regulatory departments to develop the processing standards shall not be manufactured "in Chapter 8,holister kids, Drug, and indeed in the drug factory testing links. Drug Administration did not expressly made a mandatory requirement. Sichuan Provincial Academy of Social Sciences researcher, sociologist Professor Hu Guangwei this endless shaking his head, he thought, and more from the food safety incidents such practices have proven unreliable. Nature of the firm is to maximize the benefits earned by regulatory authorities the power to release the enterprises themselves, the equivalent of "strips" can only expect manufacturers conscience, and conscience is unreliable. How much free enterprise have produced quality events. Visible in front of the interests of trust on behalf of supervision will lead into a dead letter law. "Barber is not afraid to shave his skull!" Hu Guangwei said. "We have a self-test and found no problems chromium exceeded." Office manager Anguo Yong Xiu Pharmaceutical responded by saying:. "Self-test again after the accident, but have not found chromium exceeded the problems we do not know we were exposed drugs, why would chromium exceeded. "When will the system design" prior to eliminate "too strong" after accountability " No factory clearance rights, pharmaceutical sector means that only the daily supervision. In accordance with the requirements of the Drug Administration Law, in addition to program oversight, quality evaluation of drugs, the current implementation is the sampling system. Guanghan City Secretary Food and Drug Administration Zhang Lu introduced, the council plans to do a year early, checked once every quarter, usually there are GMP inspection. If there should be ordered to report adverse reactions associated companies to accept the norms of production. In the sampling process in the council, there is no adverse reaction reports found. However sampling pass, it means all qualified Zhang Lu admitted that the council has no effect on each batch of drugs generally do Xiu Pharmaceutical factory inspection, but according to the task index higher authorities, for Xiu pharmaceutical product sampling inspection. Last year's "complex tablets and syrup fails CHUANBEIPIBA standard production",scarpe on line, this year's "excessive chromium capsules" are not found in the Council of the sampling. Hu Guangwei sociologists believe that the sampling system and the release of decentralized enterprises, are weak performance of the executive, the executive branch of human, technical means to achieve the results generally powerless to check. In Guanghan City, Food and Drug Administration, for example, to accelerate the implementation of 13 kinds of drugs allegedly excessive chrome shelves notice issued by the State Food and Drug Administration, the Bureau more than 20 employees will basically be sent to perform tasks. In their daily work,goose canada, overseeing two Xiu medicine, while also undertaking a large enterprise regulation, only to Xiu time to time to see, it is impossible 24 hours without sleep staring Xiu hold . In this regard, Hu Guangwei said that the state of the input power of administrative supervision must be strong investment in order to maintain the effectiveness of regulatory power. Other products can be sampling, but food, medicines safety of the people involved in this particular product, the use of sampling is very wrong. Some batches of drugs, missed a chance in the sampling, the lack of testing means consumers only through physical reactions after taking his own doing toxicity testing of these drugs. Although the provisions of the Drug Administration Law of the adverse drug reaction reporting system. But such a system design decisions, and all the punitive measures are accountable afterwards, but the reality of weak regulatory power of deterrence and complement to, rather than an effective means of blocking sales of pharmaceutical production problems. "W a" bound "lenient" accountable only "temporary" can solve the problem After the "poison capsule" incident was exposed, the relevant departments to act quickly, a large number of raw material manufacturer is inventory, personnel were controlled enterprises were halted. Xinchang 23 suspects were taken criminal coercive measures, Hebei Fucheng County gelatin enterprise-wide suspend production for rectification. These sources all have similar characteristics: inferior to bring low-cost, scale dumping bring qualification to bring protection. In particular qualification problems,hollister, many involving pharmaceutical companies are screaming injustice: we purchase are formal channels are from qualified companies into the goods. We review the results right suppliers shall be held responsible reserved. In fact, the fundamental problem is not the source. Finished "wide out" will inevitably lead to raw materials "lenient." If exports truss, the elimination of the finished product and more, companies with low-quality low-cost raw material can not be obtained profits,chemise hollister, the companies themselves will afterwards, will increase the critical raw materials, poor quality products will lose market. Instead, factory areas,hollister sale, all the way to the green, even if there is accountability afterwards, can not stop the immediate temptation. In front of the profits, is there any way to restrain corporate profit-driven impulses, not to pick cheaper raw materials it Anyway, own their own investigation. Known as the "king of generic drugs," the Xiu medicine, core competence is low and scale of the accident amoxicillin capsules, in Guanghan local market price per edition is only a dollar, while other pharmaceutical companies Amoxicillin price is around five dollars. Unconscionable making materials "temporary", indeed should be severely hit, but only hit the source is not enough, should truss exports. If the pharmaceutical factory release system not well resolved,goose outlet, then there will always be a market downstream manufacturers upstream "temporary", "small workshop" match up,abercrombie, providing the raw material of unknown origin. As long as the price is low enough, low to the conscience of the following, as long as the profit is high enough, high enough to block the self-test eyes. 相关的主题文章：