随着《药品管理法》的实施,药品监督工作正由事后管理向事前管理的方向转化。那么,怎样才能有效的进行事前管理,把假劣药品查处在产生和造成的危害之前呢?我们认为,不仅要组织突击性的大检查和传统的抽检,查处已出现的违法案件,更重要的是要对药品生产、经营企业、制剂单位进行经常性的、科学化的考查。 With the implementation of the Drug Administration Law, pharmaceutical supervision is being transformed from ex-post management to ex-management. So, how can we carry out effective management in advance and investigate and deal with counterfeit drugs before the harm caused and caused? We think it is not only necessary to organize a large surprise checkup and a traditional sampling inspection, investigate and deal with illegal cases that have emerged, but more importantly It is necessary to conduct regular and scientific examination of pharmaceutical production, management enterprises and preparation units.