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国家药品监督管理局在药品管理法修订草案中重新界定了假劣药品。有下列情形之一的药品按假药处理:①国务院药品监督管理部门规定禁止使用的;②未取得批准文号或者未经批准配制的;③变质不能药用的;④被污染不能药用的;⑤进口的药品未经批准或者未经授权的药品检验机构检验的;
State Drug Administration in the revised draft drug administration law redefined the counterfeit drugs. Drugs that are under any of the following circumstances are handled as counterfeit medicines: ① Prohibited to be used by the drug regulatory department of the State Council; ② No approval number or preparation without authorization; ③ Modification can not be used medicinally; ④ Polluted and non-medicinal ; ⑤ imported drugs without approval or unauthorized drug testing agency inspection;