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药品监督检验档案,是指在药品监督管理和检验过程中所形成的具有一定法律效力的文件和技术资料。它是一种专业性科技档案,对药品的监督管理和检验有十分重要的凭证和参考作用。过去药品监督检验档案没有统一的管理标准,给档案的管理、统计、利用、交流造成很大不便,实践证明,实现药品监督检验档案规范化管理不仅有助于提高手工管理的水
Drug supervision and inspection files, refers to the drug supervision and management and inspection process formed by a certain legal validity of the documents and technical information. It is a professional science and technology files, the supervision and management of medicines and testing have very important evidence and reference. In the past, there was no unified management standard for drug supervision and inspection archives, causing great inconvenience to the management, statistics, utilization and exchange of archives. Practice has proved that the standardized management of archives for drug supervision and inspection not only helps to improve the manual management of water