| 陈亚飞,刘明理,谢晶鑫,赵宗阁,张学博,吴先富,曹丽梅,肖新月.药品标准物质的管理与研制生产质量控制[J].中国药事,2018,32(11):1505-1510 |
| 药品标准物质的管理与研制生产质量控制 |
| On Management of Pharmaceutical Reference Standards and Quality Control for Research and Production |
| 投稿时间：2018-04-25 |
| DOI：10.16153/j.1002-7777.2018.11.009 |
| 中文关键词: 药品标准物质 研制生产 质量控制 |
| 英文关键词: pharmaceutical reference standards research and production quality control |
| 基金项目: |
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| 摘要点击次数: 1546 |
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| 中文摘要: |
| 目的：介绍药品标准物质管理的组织结构与研制、生产和分发中的质量控制要求，为药品标准物质的质量和供应提供更好的保障。方法：基于ISO 17034国际标准要求，梳理药品标准物质研制、生产与管理工作流程，分析研制生产与管理各环节中应控制的质量要素，强调遵循规定要求的重要性。结果：建立和完善药品标准物质研制、生产和管理的质量控制和持续供应的有效机制。结论：为确保药品标准物质的质量和可获得性，加强药品标准物质各流程环节管理很有必要。 |
| 英文摘要: |
| Objective: To introduce the management organization structure and quality control requirements for the research, production and distribution of pharmaceutical reference standards in order to guarantee the quality and supply. Methods: The research, production and management workflow for pharmaceutical reference standards were analyzed based on the requirements of ISO 17034 international standards. The quality factors that should be controlled in all aspects of research, production and management were also analyzed. The importance of complying with the requirements was emphasized. Results: An effective mechanism for the quality control of the research, production and distribution and continuous supply of pharmaceutical reference standards was established and improved. Conclusion: In order to ensure the quality and availability of pharmaceutical reference standards, it is necessary to strengthen the management of each process of workflow of the pharmaceutical reference standards. |
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