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    Home > Biochemistry News > Plant Extracts News > Drug administration investigates and deals with the problem of Chinese Herbal Pieces

    Drug administration investigates and deals with the problem of Chinese Herbal Pieces

    • Last Update: 2013-10-18
    • Source: Internet
    • Author: User
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    On October 15, the State Food and Drug Administration announced the special spot check of the dyeing problem of Chinese herbal pieces There were 22 batches of Honghua, yanhusuo and xihonghua with dyeing problem The local drug regulatory departments were required to investigate and deal with the Chinese herbal pieces and related units with dyeing problem according to law Among them, 7 batches of safflower and yanhusuo, which were operated and used by 2 retail pharmacies and 1 medical institution in our city, were found to have dyeing problems in sampling inspection According to the information on the website of the State Food and drug administration, the three operating and using units involved in our city are Sungang drugstore of Shenzhen Asia drugstore chain Co., Ltd., Fuhua drugstore of Shenzhen Youhe pharmaceutical chain Co., Ltd and Shenzhen traditional Chinese medicine hospital It is reported that the Municipal Food and drug administration has filed a case investigation on the three operating and using units involved in the city, ordered them to stop operating and using the problem products immediately, and traced the source of production Through preliminary investigation, 7 batches of unqualified products operated and used by 3 operating and using units involved in our city are all produced by foreign enterprises producing Chinese herbal pieces, the source of product purchase channels of 3 units is legal, and all of them are from foreign legal pharmaceutical production and operation enterprises, and the SFDA has coordinated the local pharmaceutical supervision department to investigate and deal with the source At the same time, a notice of investigation and punishment was issued on the website of the Bureau, requiring all drug handling enterprises and medical institutions in the city to carry out self-examination on the notified problematic products If any defective products are found, they shall be immediately stopped from operation and reported.
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