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我国《药品管理法》的颁布实施,使药品管理由行政管理进入法制管理,对药检所的质量监督检验工作提出了新要求.面对新的形势,我们认为要做好当前药品质量监督检验工作有很多问题值得探索.为此我们按照《药品管理法》的有关规定,结合江苏医药卫生事业的实际,围绕执法,对药品质量监督检验工作进行了一些初步改革,以期更好地完成我省药品质量监督检验任务.一年来的实践表明,我们的偿试取得了初步成效,基本上达到了预期目的.现将我们的实践和体会总结如下:
The promulgation and implementation of the “Drug Administration Law” in our country has enabled the drug administration to enter the legal system administration from the administration and put forward new requirements for the quality supervision and inspection of the drug administration. In the face of the new situation, we think that we should do a good job in the current drug quality supervision and inspection There are many problems worth exploring.Therefore, we follow the relevant provisions of the “Drug Administration Law”, combined with the actual medical and health care in Jiangsu Province, around the law enforcement, drug quality supervision and inspection carried out some preliminary reform, with a view to better completion of our province drugs Quality supervision and inspection tasks.Over the years of practice shows that our trial has achieved initial results, basically achieved the desired purpose. Now our practice and experience are summarized as follows: