EPCIS规范允许使用关于供应链中的标记药品的上下文信息增强来自原始读事件的信息。
The EPCIS specification permits the data from raw read events to be augmented with contextual information about the observation of tagged items in the supply chain.
负责药品、医疗器械行政监督和技术监督，负责制定药品和医疗器械研制、生产、流通、使用方面的质量管理规范并监督实施。
To formulate and revise norms for the quality management of drug research, manufacturing, distribution and use, and supervise their implementation.
目的探讨肿瘤病区高危药品使用流程，严格规范化管理，促进肿瘤病区护理用药安全。
Objective To investigate the process of tumor ward high-risk drug use, strict standardized management, the promotion of cancer ward nursing medication safety.
前言： 目的：评价药品包装、标签和说明书规范后的执行情况及其在使用过程中仍然存在的问题。
Objective: To analyze the questions about the package, labels and specifications of drugs after they had been authoritatively stipulated.
前言： 目的：评价药品包装、标签和说明书规范后的执行情况及其在使用过程中仍然存在的问题。
Objective: To analyze the questions about the package, labels and specifications of drugs after they had been authoritatively stipulated.
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