随着国家药品监督管理局成立，政府部门职能的调整，修订《药品管理法》已是当务之急，笔者提出以下建议供参考。１　关于药品批准文号的管理药品批准文号是国家有权机关按照法定标准、生产工艺和生产条件对特定企业生产特定药品的资格认定。药品批准文号的管理在整个药品监督 With the establishment of the State Drug Administration and the adjustment of the functions of government departments, it is imperative to amend the Drug Administration Law. The following suggestions are made for reference. 1 on the drug approval number management of drug approval number is the state organs of authority in accordance with statutory standards, production technology and production conditions for a particular enterprise to produce a specific drug eligibility. Drug approval number management throughout the drug supervision