Beijing canceled the nine pharmaceutical companies bidding qualification will be a thorough investigation of the problem capsule

19, part of the display of the Ningxia Yinchuan City Drug testing laboratory assistant seized capsules. Local law enforcement officers, and ended on the 18th, Ningxia seized a total chromium content exceeding 1 262 boxes of capsules, have been archived processing. Xinhua News Agency issued
with the” poison capsule after another off the shelf. Yesterday, the Chongwenmen a pharmacy shelf last few formal capsule. The Beijing News reporter Zhou Gangfeng photo
18 , Baqiao District the Zaoyuan Su village uninhabited hillside was dumping a lot of empty capsule. Baqiao District Food and Drug Administration staff said that the analysis does not rule out the possibility that black workshop production of poor quality empty capsule. Law enforcement officers have the capsule shell archive, for further investigation. Dong Guoliang photo strictly prevent

, industrial gelatin used for the production of pharmaceutical capsules, to prevent the chromium exceeded medicinal capsule into the pharmaceutical manufacturing enterprise, to prevent chromium exceeded the production of drugs into the market of medicinal capsules. Firmly control the destruction of substandard products. – The State Food and Drug Administration

Beijing News News Beijing yesterday full stop 9 exposure production of capsule products. According to the identified, the State Food and Drug Administration recently released by the substandard products, the Beijing a total of 10 batches of seven varieties of sales.

Beijing Food and Drug Administration, said the nine pharmaceutical companies will be included in the Beijing pharmaceutical bidding “black list” means the production of all drugs are not in Beijing to participate in the tender. With immediate effect, the sampling will be the city’s all pharmaceutical medicinal hollow capsules.

the 10 batch problem capsule sale

problem capsule after exposure, in accordance with the provisions of the State Food and Drug Administration, on the 16th Beijing has announced the suspension of 13 batches of the sale of nine companies drugs. However, in the evening on the 19th, the State Food and Drug Administration announced the first batch of sampling results of the “poison capsule, according to inspection reports, nine drug manufacturers tested 33 varieties of 42 batches of products, of which 23 batches qualified batches of substandard products and types of all to expand exposure than CCTV.

Yesterday, the Beijing Municipal Food and Drug Administration, in accordance with the requirements of the State Food and Drug Administration issued an emergency notice, the overnight deployment Drug Administration to take measures.

reporter learned that the City Food and Drug Administration to identify, through the start of the Beijing Municipal Drug traceability system for the 14 varieties of the State Food and Drug Administration recently released by the nine companies in 23 batches of substandard products, Beijing 10 batches of seven varieties of drugs on the market for sale.

this, the county Drug Administration has notified the medical institutions, drug wholesalers, pharmacies stop selling the batch on the use of drugs, and in accordance with the Drug Recall Measures for the Administration and supervision of enterprises drug recall.

pharmaceutical companies into the tender “blacklist”

Beijing Food and Drug Administration, introduced yesterday failed batch released by the 9 Exposure of pharmaceutical production capsule formulation of drugs, all within the city, off the shelf and immediately stop the sale and use.

the same time, in accordance with the relevant provisions of the Beijing pharmaceutical bidding, nine drug manufacturers will be included in the pharmaceutical bidding “blacklist”, the production of all drugs were abolished in Beijing to participate in the drug tender qualifications. Beijing will also strengthen the drug companies involved in bidding qualification examination.

Beijing medicinal hollow capsules enterprise. “Yesterday, the City Drug City Drug in pharmaceutical production processes, have been carried out on the capsule formulation of Beijing all varieties of full-coverage check.

City Food and Drug Administration requirements, such as found in the capsules to buy into the capsule from the origin in Zhejiang and other enterprises be stopped; found to have been made drugs, ordered the recall, and drugs all involved archive, investigated and dealt with according to law.

In addition, now, Beijing has begun production of capsule dosage form drug companies medicinal hollow capsules testing detection, and full implementation of the verification found substandard products will be investigated and dealt with according to law.

visit

problem Capsule “drugstore shelf

Last night, the reporter visited a number of pharmacies, 14 kinds of chromium content than the national pharmacopoeia limits of the capsule drugs, have the shelf sale.

the Guangqumen rich Park Avenue, near a pharmacy, the reporter asked whether there Sichuan Sichuan pharmaceutical production of amoxicillin, the clerk replied that “not to sell” For non-prescription drugs, excessive chromium content in the most serious the Tonghua Yisheng Pharmaceutical Co., Ltd. Yan Li Xiao Capsule (test results 149ppm) has been off the shelf. Who Tonghua Yi Sheng the Tonghua Sheng and medicine, can not sell. “

in the East Flower Market Street, a small western medicine pharmacies, any brand of amoxicillin, Li Xiao Yan, Weikangling such as capsules, no sales.

Yesterday, the reporter called gold 5 stores like pharmacy Dongcheng, Xicheng, Fengtai, asking the capsules of the pharmaceutical companies named by the Food and Drug Administration, the answer is “off the shelf”, including the right Tiananmen Square on duty of a store shelf yesterday afternoon received a notice.

■ initiatives

Food and Drug Administration: “The problem Capsule” resolutely control the destruction of

deployment medicinal capsule quality and safety special supervision and inspection operations, the scope to cover all drugs capsule enterprise

Beijing News News yesterday, the State Food and Drug Administration held a teleconference meeting, deployment, supervision and inspection of medicinal capsule quality and safety special action required to prevent industrial gelatin for the production of pharmaceutical capsules, to prevent chromium exceeded medicinal capsule into the pharmaceutical manufacturing enterprises into the market. The State Food and Drug Administration requires provinces to seriously investigate and deal with the companies involved, firmly control the destruction of substandard products.

State Food and Drug Administration requirements, the provincial Food and Drug Administration immediately organized to carry out supervision and inspection of all medicinal gelatin and medicinal capsule manufacturers, focusing on checking the source of raw materials, supplier audits, incoming inspection, factory inspection the whereabouts of product sales, with or without the use of industrial gelatin, etc.; immediately organized to supervise and inspect all capsule formulations of pharmaceutical production companies, focusing on checking the source of medicinal capsules, supplier audit, and incoming inspection.

In addition, drug manufacturers from the hollow capsules enterprises involved in the purchase of substandard medicinal capsule in-depth inspection, identification of all varieties and batches, and to take immediate inquiry and control measures; immediate area of ??medicinal production of gelatin gelatin manufacturers, Medicinal hollow capsule production and production of capsule comprehensive sampling. Market the testing of the capsule formulation of drugs, the implementation by the National Bureau of unified organization.

In addition, the State Food and Drug Administration found substandard medical gelatin in the supervision and inspection, Medicinal hollow capsule, the capsule formulation of drugs, food and drug regulatory authorities in accordance with the law dealt with severely.

Ministry of Health: medical institutions inventory problem capsule

stop the purchase and use of multi provinces poison capsule shelves archive

new Beijing reported hearing the Ministry of Health yesterday’s news, the Ministry of Health on April 19 issued a notice of the medical establishment to carry out an inventory check for exposure “problem capsule products, inventory and use of drugs, and stop the purchase and use.

the

the person concerned of the State Food and Drug Administration said the newspaper everywhere thorough investigation of the capsule drugs, sampling will not be limited to this group will not be limited to nine companies.

inventory range updated after a new batch of “Capsule” on the list of exposure, the person concerned of the Ministry of Health said last night, the Ministry of Health will adjust the inventory based on the latest list published by the State Food and Drug Administration the scope of the inspection.

At present, the place has begun to conduct a serious investigation of the problem capsules, including Beijing, Tianjin, Chongqing, Zhejiang, Jiangsu, Gansu and other provinces (cities, districts) problem capsule to the next frame, sealed.

at the same time, the Food and Drug Administration issued a document, said the issue of the Bulletin capsule, has instructed the enterprises where the provincial Food and Drug Administration, the seizure of the above enterprises capsule formulation of production sites, and ordered to the above companies immediate recall test failed batch times drugs. Destroyed by the supervision of the local food and drug supervision departments. Why

■ survey

“blacklist” of enterprises repeatedly committing the crime?

Zhejiang Xinchang two capsules instead of pharmaceutical gelatin production plant with industrial gelatin capsules, two on the “blacklist”

as early as last year, spot checks in the local pharmaceutical sector sacked, “the two enterprises in Xinchang County, Zhejiang recently investigated the problem capsule event, because of suspicion of production and sales of toxic, harmful Medicinal hollow capsule, appear in the list of companies, was closed down. Should the government focus on monitoring the scope of the “blacklist” of enterprises, why dare to repeatedly commit crimes?

seizure of the enterprise had a criminal record

ended at 8:00 on the 17th, the public security organs in Xinchang County has 23 criminal suspects taken criminal coercive measures, total seizure involved in the production of capsules 4 the Xinchang Zhuokang China Star, Daphne, Raymond Limited. Tellingly, four enterprises in the seizure of the two, in fact, has long been included in the “blacklist” of the local pharmaceutical sector.

Xinchang Food and Drug Administration, Deputy Secretary Kongding Hong said in last year’s sampling found 12 cases of capsule enterprise of raw materials and products violations, the seizure Zhuokang Capsule Co., Ltd. and China Star capsules plant, discovered last year that chromium exceeded, be punished by a fine and confiscation of raw materials, products punishment.

It is understood, not large-scale two capsules plant of the Zhuokang Capsule Co., Ltd. and China Star just Xinchang Capsule enterprise, with an annual value of about 10 million yuan, while the local best efficiency of capsules plant output can reach NT $ 100 million.

companies in Zhuokang, the reporter saw the finished goods warehouse is strewed with edible gelatin and gelatin raw materials and packaging boxes of capsules finished. Chinese Star capsule plant closed the door, has been labeled a seal.

Xinchang County, a total of 43 Capsules for pharmaceutical manufacturers, the annual output capsule 100 billion, accounting for about one-third of the country’s medicinal capsule production. In the town of Confucian Ao capsule industry accounted for more than 40 percent of the local fiscal revenue.

because the problem capsule events, all capsules enterprises in the county to suspend production for rectification. Xinchang Confucian Ao town reporters on the 17th came to be known as “hometown of capsules, see all capsule manufacturers have been lay-off factory worker’s, and even the street capsules, gelatin wholesale The shop is no longer operating.

inadequate supervision lead to the “desperate”

reporter learned in the investigation, only the low-cost map bidding mechanism causes the enterprises have to do everything possible to suppress the capsule price, creating a vicious competition. Xinchang Canton of Vaud capsules Stone, general manager, said Hodo, medicinal gelatin and industrial gelatin prices are quite different, the price of pharmaceutical gelatin 1 ton to more than 50,000 yuan per million capsules ex-factory price is generally 90-100 yuan ; industrial gelatin price of 1 ton is about 2.5 million per million capsules ex-factory price of about $ 40 cheaper than the capsule of pharmaceutical gelatin production.

industry can separation of pharmaceutical gelatin and industrial gelatin. Million capsules, pharmaceutical gelatin profit only a few dollars, and now pharmaceutical companies to lower prices through various means, or some small businesses simply can not survive.

Xinchang Food and Drug Administration, Deputy Secretary Kongding Hong said that, in accordance with the provisions of the Drug Administration Department is responsible for the regulation of pharmaceutical gelatin, the quality supervision department is responsible for monitoring food gelatin. The production of capsules of raw materials for pharmaceutical gelatin, if the enterprise is using edible gelatin, as long as the chromium content is not excessive, still belong to the legitimate range, so monitoring is difficult. Drug Administration Department each year for local businesses generally twice sampling is divided into planned inspection and spot checks by the end of March early April this year, the first sampling, the results are not yet out.

In addition, the local regulatory authorities to check without Department penalty rather lax. Kongding Hong introduction, sampling enterprises, in accordance with the provisions of relevant laws, only, respectively, were sentenced to the punishment of 20000-50000 yuan confiscated raw materials and finished goods were destroyed. A capsule manufacturers told reporters: ‘sampling’ caught ‘on the’ blacklist ‘loss Chengsi than 10 million, with 34 tons of industrial gelatin instead of pharmaceutical gelatin put the money back. “

government regulators should have independence in

a large pharmaceutical company responsible person said, in drug surveillance efforts to disciplinary punishment is far to keep up with the attractiveness of the profits of the manufacturers again and lead to portions of capsules and again three criminal.

Zhejiang Academy of Social Sciences Research Center Director Yang Jianhua recommendations, we must first maintain the independence of the regulators, the complete elimination of the regulators and the regulated objects coexist and improve the credibility of the primary regulatory enforcement; to clarify the department responsible enrich the primary regulatory power, to build a more comprehensive and effective regulatory system from the perspective of the whole industrial chain. According to Xinhua News Agency

respond

problem capsule recall inventory capsule archive

Tonghua Gold Horse not found in the capsule and all recall; two pharmaceutical companies a public apology

Beijing News News chromium exceeded the capsule sampling results yesterday, arising from either of the Tonghua Gold Horse, Yisheng Pharmaceutical companies at the official website to hang out in the State Food and Drug Administration announced progress notice, and clearly caused apology.

inventory capsule seal up

Tonghua Gold Horse “problem Capsule” attributed to “accidentally select the” capsule supplier. Said, adding that only focus on the supplier’s qualification certificate and over-confident that the inspection report of the supplier of the product, the lack of depth of vendor products should be understood that the neglect of the quality testing of the capsule into the factory.

the

company also said it will be the company capsules existing stocks of finished goods, semi-finished products, packaging and production line of local archive, purchase from other manufacturers have not yet found all capsule products from the market throughout the country all recall, sent to the drug regulatory departments at a higher level re-tested capsule quality.

In addition, Tonghua Gold Horse yesterday for the first time to apologize, saying “this incident, the impact on consumers and the general public to express my deep apology.”

However, as of last night 8:00, as the A-share listed companies, Tonghua Gold Horse has not been designated by the CSRC disclosed the platform to release any announcement to investors. Yesterday’s close, the company’s shares fell 1.63 percent, to close at 4.84 yuan. The company’s shares have floating green in which the trading of more than previously. “Impact on first quarter results.” The company’s securities department official, told reporters that regulators are still factory survey, the impact of the situation is still not enough to make an announcement. Attainment of “based on specific identification and impact, to choose whether to consult the Exchange in the future.”

a number of pharmaceutical companies to recall the drug capsules

the same yesterday, Tonghua Yisheng Pharmaceutical hang out at the official website of the “letter of apology.” According to the sampling results of the State Food and Drug Administration, its production of “Yan Li Xiao capsule chromium exceeded in nine of the most serious, about 70 times. Yi Pharma said that the harm to the consumer medication safety, we feel very sad, and deeply apologize to the vast number of consumers, the whole society to apologize.

reporter yesterday called several other arising from either pharmaceutical companies, the the Qinghai Glasgow Dandong Pharmaceutical responsible for sales, sources said, identified batch recall, other capsule products be suspended, and is in the process of being recalled. The Xiu Pharmaceutical involved batches of capsules have been recalled.

doubts

39 categories of food can not add gelatin

national food security assessment center experts yesterday explained that edible gelatin is China allows the use of food additives, mainly functions as a thickener. Industrial gelatin, however, does not belong to the scope of food additives, industrial gelatin for use in foods is an offense, the potential problem is the problem of heavy metal pollution and other hazards to human health,

At present, China has industrial gelatin into the food may be illegal to add non-food list of substances “.

the expert interpretation of edible gelatin, nor can be used in all food categories, According to regulations, can not be used, including pasteurized milk, sterilized milk, fermented milk, milk powder, rice, honey 39 of the infant formula food, drinking water, fruit and vegetable juices, wine, tea, coffee and other food category.

A08-A09 version written (except for signature outside)/Beijing News reporter Wen Ru Wu Peng Liu Xia Liu Jenny

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