【摘要】：對我國實施獸藥生產(chǎn)質(zhì)量管理規(guī)范以來獸藥生產(chǎn)許可管理的發(fā)展情況進(jìn)行了簡要回顧和總結(jié),分析了獸藥生產(chǎn)許可和GMP申報審查工作中遇到的常見問題,并對今后進(jìn)一步做好獸藥生產(chǎn)許可管理工作提出思考和建議。
[Abstract]:This paper briefly reviewed and summarized the development of veterinary drug production license management since the implementation of the veterinary drug production quality management standard in China, and analyzed the common problems encountered in the veterinary drug production license and GMP application examination. The author also puts forward some thoughts and suggestions on the management of veterinary drug production license in the future.
【作者單位】： 中國獸醫(yī)藥品監(jiān)察所;
【分類號】：F426.72
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本文編號：2219591