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当前,我国药品安全问题层出不穷,特别是近年来一些大型药企、知名药企丑闻频发,对人民群众的健康安全和社会和谐稳定造成了不利影响,亟待相关部门进一步加强监督管理。档案工作是药品监管过程中的基础工作之一,必须始终高度重视、认真对待、深入研究,不断加大工作力度,切实加强新形势下药品监管档案工作。一、药品监管档案工作的重要性分析1.药品监管档案是医药卫生档案的重要部分。药品监管档案包括与药品相关的法
At present, there are an endless stream of drug safety problems in our country. Especially in recent years, some large-scale pharmaceutical enterprises and well-known pharmaceutical enterprises have been causing frequent scandals, adversely affecting the people’s health and social harmony and stability and urgently requiring relevant departments to further strengthen supervision and administration. Archives work is one of the basic work in the process of drug supervision. We must always attach great importance to it, take a serious look at it, study it in depth, increase our efforts and conscientiously strengthen the archives work under the new situation. First, the importance of drug regulatory file analysis 1. Drug regulatory file is an important part of the medical and health files. Drug regulatory files include drug related law