论文部分内容阅读
为认真贯彻落实国务院领导关于把药品监督管理工作作为重点抓紧抓好的指示,全面履行国务院赋予的对药品研究、生产、流通、使用全过程进行监督管理工作的职责,确保人民用药安全有效,国家药品监督管理局日前制订了1999年的全国药品抽样检验工作计划,提出八项药品抽样检验工作重点。①新批准生产和试生产转正式生产的药品、中药保护品种、医疗单位配制制剂、进口药品、生物制品、血液制品。通过GMP
In order to conscientiously implement the instructions of the State Council leadership on taking pharmaceutical supervision and management as a key priority and fully implement the responsibilities assigned by the State Council for supervision and administration over the entire process of drug research, production, distribution and use, and ensure the people’s medication is safe and effective, Drug Administration recently formulated a national drug sampling inspection work plan in 1999, proposed eight drug sampling inspection focus. ① newly approved the production and trial production into formal production of drugs, traditional Chinese medicine protection varieties, medical units preparation of preparations, imported drugs, biological products, blood products. Through GMP