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    Home > Medical News > Latest Medical News > Three pharmaceutical companies lost their GSP certificates and 30 cancelled their production licenses

    Three pharmaceutical companies lost their GSP certificates and 30 cancelled their production licenses

    • Last Update: 2016-11-08
    • Source: Internet
    • Author: User
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    It is reported that Hubei, Anshan and Beijing food and Drug Administration issued an announcement to withdraw the GSP certificate of one pharmaceutical enterprise, cancel two, and cancel the medical device production license of 30 enterprises Details are as follows: Hubei Hubei Lisheng Pharmaceutical Co., Ltd., in violation of the provisions of the regulations on the quality management of Pharmaceutical Trading (Order No 13 of the State Food and Drug Administration), and in accordance with the provisions of Article 25 of the measures for the flight inspection of pharmaceutical and medical devices (Order No 14 of the State Food and Drug Administration), Hubei food and Drug Administration decided to take back the drug of Hubei Lisheng Pharmaceutical Co., Ltd Certificate of operation quality management standard Now, the relevant information of Hubei Lisheng Pharmaceutical Co., Ltd is published (see Annex) Relevant information of enterprises with GSP certificate withdrawn (2016 No.6) Anshan Deshuntang pharmacy in Niuzhuang Town, Haicheng City, and kangditang pharmacy in Gengzhuang Town, Haicheng City, have seriously violated the provisions of the pharmaceutical trading quality management specifications According to the provisions of Article 45 of the measures for the administration of the certification of the pharmaceutical trading quality management specifications, Anshan food and drug administration has revoked its two certificates of the certification of the pharmaceutical trading quality management specifications in accordance with the law, which are hereby promulgated Since the third quarter of 2016 in Beijing, 30 medical device manufacturers in Beijing have been cancelled their licenses for actively applying for cancellation of medical device production license (hereinafter referred to as "license") and not applying for extension within the validity period of the license It is hereby announced as follows: 1 A total of 10 medical device manufacturing enterprises (see Annex 1) take the initiative to apply for cancellation within the validity period of the license According to Article 23 of the measures for the supervision and administration of the production of medical devices (Order No 7 of the State Food and Drug Administration), the Bureau will cancel their medical device manufacturing licenses according to law 2、 A total of 20 medical device manufacturers (see Annex 2) failed to apply for extension within the validity period of the license The Bureau cancelled their medical device production licenses according to Article 17 of the measures for the supervision and administration of medical device production (Order No 7 of the State Food and Drug Administration) Details are as follows: Appendix 1: list of enterprises applying for cancellation initiatively Appendix 2: list of enterprises not applying for extension according to law
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