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《药品管理法》的实施,标志着药品管理走上了法制化的轨道.作为药品监督管理事业组成部分的药品检验工作也应有符合《药品管理法》要求的运行轨道.应当运用有计划、讲效率的工作方法、从事药品质量的监督与检验.近二、三年来,我所在药品检验工作规范化方面进行了一些探索,现介绍如下:一、规范化的初步设想:从总结多年药检工作的实践经验中,我们对药品质量监督检验,检查工作规范化的设想是:规定一定的工作周期(一般以年为单位);规定每一周期中必须进行的工作如:有关药品质量监督检验、检查及其信息的收集、加工、应用等,规定这些工作的对象、范围、数量和质量要求,进行的方式以及结果处理程序等.
The implementation of the Drug Administration Law marks that drug administration has embarked on the track of legalization.Checking for drugs that is part of the drug supervision and management business should also have a track for compliance with the requirements of the Drug Administration Law.It should be implemented in a planned, The efficiency of the working methods, the quality of drug supervision and inspection in the past two or three years, I am in the standardization of pharmaceutical inspection carried out some of the exploration are presented below: First, the standardization of the initial idea: from the summary of years of practice of drug testing work In our experience, we envisaged the standardization of drug quality supervision, inspection and inspection as follows: stipulating a certain work cycle (usually in terms of years); stipulating the work to be carried out in each cycle such as: inspection and inspection of drug quality supervision and inspection The collection, processing and application of information, etc., stipulate the objects, scope, quantity and quality requirements of these tasks, the methods of implementation and results processing procedures.