National Food and Drug Administration recently reported，Chromium Excessive Capsules Drugs Basically Checked，The results of the sampling inspection have been from the relevant province (district、City) Food and Drug Administration announced through the website，and summarize it on the website of the State Food and Drug Administration。
 
Chromium over -the -standard pharmaceutical capsule incident，Party Central Committee、Leaders of the State Council attach great Stake Sports Bettingimportance to，Requires to carefully check and disposal according to law，Timely respond to social concerns，Resolutely block supervision vulnerabilities，Effectively safeguard the health rights and interests of the masses。The State Food and Drug Administration organizes mobilization full system forces，Comprehensively carry out the supervision and inspection of enterprises and product drawing，Time to control the problem product。hygiene、Business and other departments actively cooperate with the recall of product recall of chromium exceeding the standard。After more than 1 month of work，At present, the drug situation of chromium exceeding standard capsules is basically checked。For the newly listed 4374 batches of capsule drugs after May 1st，The test results are all qualified。Capsule drugs produced before April 30，Order the manufacturer to self -check in batches，The batch of enterprise self -inspection has reached about 90,000 batches，Found that chromium exceeding the standard has taken the initiative to get off the shelves、Seal、Recall and destroy。At the same time，The State Food and Drug Administration organized a sampling test to 1993 companies producing capsules in the country，Sample inspection covers all capsule drug production enterprises。As of May My stake betting app24，Pharmaceutical inspection institutions at all levels have drawn a total of 11561 batches of capsules drugs，Qualified products of chromium content within the prescribed standard 10892 batches，account for 94.2%，669 batches of unqualified products with exceeding chromium content，5.8%。254 manufacturers with chromium excessive drug problems，12.7%of all capsule drug production enterprises。The State Food and Drug Administration requires local governments to immediately organize the sampling test and find that chromium exceeds the standard、Seal、Recall and destroy。At the same time，A batch test for other batches of capsules produced by the enterprises produced by these drugs，Those who pass the test can continue to be sold，Check out immediately for inspection、Seal、Recall and destroy。
 
National Pharmacopoeia Standard stipulates that the limited value of chromium content is two -millionth，The purpose is to strictly prohibit the use of pharmaceutical capsules for the use of leather manufacturing。The Capsule Drug Pharmaceutical Chromium Excessive Question，The main reason is that capsule manufacturers illegally purchased and used Gelatin -made medicinal capsules produced by leather，and sell it for drug production enterprises; at the same time，Some pharmaceutical manufacturers violate laws and regulations and Stake Sports Bettingdrug production quality management specifications，Use unqualified accessories to produce inferior drugs。For the above behavior，All shall be dealt with seriously in accordance with relevant laws and regulations。
 
The State Food and Drug Administration has requested that all places to find out the illegal facts of the problem enterprise as soon as possible，Consident investigation and punishment in accordance with the Drug Management Law and relevant laws and regulations，The suspected crime is handled by the public security organs in accordance with the law。Current，236 of the capsule drug production enterprises in various places，Discontinued production and rectification 42，84 seizes production lines; 7 drug production licenses of pharmaceutical capsules; transferred to public security organs to handle gelatin and capsule manufacturers。I also found it in the investigation of the case，Some companies illegally produced and sold medicinal gelatin and capsules without permission，Relevant departments have taken decisive measures to punish in accordance with the law。
 
Requirements for the State Food and Drug Administration，Food and drug supervision departments at all levels summarize lessons，Find vulnerability，Against three，Strengthen supervision，Implement responsibility，Further improve the long -term mechanism of drug supervision，My stake betting appStrengthen the construction of drug supervision capabilities and daily supervision，Event such problems happen again，Ensure the safety of public medication。