药品质量检验及标准化管理探析  

Analysis of Drug Quality Inspection and Standardized Management

作　　者：韩勇 杨雪姝 杨婷 HAN Yong;YANG Xueshu;YANG Ting(Panxi Vanadium and Titanium Inspection and Testing Institute,Panzhihua 617099,China)

机构地区：[1]攀西钒钛检验检测院,四川攀枝花617099

出　　处：《品牌与标准化》2024年第6期142-144,共3页

摘　　要：随着我国医疗技术的飞速发展和药品种类的逐渐丰富,药品质量的提升成为保障患者生理和机体治疗要求的关键因素。在这一背景下,药品质量检验方法及标准化管理方式的研究显得尤为迫切。本文将从药品质量检验的方法论和管理体系两个方面入手,深入挖掘药品质量控制的关键环节,为药品生产和检验工作提供科学的指导和依据。通过对相关文献的综合分析和案例研究,为药品行业的从业人员提供实用的经验和建议,以推动我国药品质量管理水平的提升。With the rapid development of medical technology and the gradual enrichment of drug types in our country,the improvement of drug quality has become a key factor in ensuring the physiological and therapeutic requirements of patients.In this context,the research on drug quality inspection methods and standardized management methods is particularly urgent.This article will start from the methodology and management system of drug quality inspection,delve into the key links of drug quality control,and provide scientific guidance and basis for drug production and inspection work.Through comprehensive analysis of relevant literature and case studies,provide practical experience and suggestions for practitioners in the pharmaceutical industry to promote the improvement of drug quality management level in China.

关 键 词：药品 质量检验 方法 标准化管理 

分 类 号：F203[经济管理—国民经济] F426.72F273.2