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摘要:
Objective To study the origin and development,framework and content of the EU-RMP(European Drug Risk Management Plan)so as to provide a reference for China’s drug risk management plan(RMP).Methods Literature research and comparative research were used in this paper.Through searching Chinese and foreign literature,the website of European Medicines Agency(EMA)and the Guideline on Good Pharmacovigilance Practices(GVP),in-depth understanding of the EU-RMP content and requirements,some lessons were extracted for our reference.Results and Conclusion All departments should cooperate closely in the preparation of RMP in China.Then,the risk control measures should be further enriched to reduce the risks.Besides,the rules for implementing RMP should be clarified to promote the risk management of the whole life cycle of drugs and maintain the safety of patients’medication.
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篇名 Research and Enlightenment of EU Drug Risk Management Plan
来源期刊 亚洲社会药学 学科 医学
关键词 risk management plan risk minimization EU
年,卷(期) 2021,(1) 所属期刊栏目
研究方向 页码范围 23-30
页数 8页 分类号 R73
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risk
management
plan
risk
minimization
EU
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亚洲社会药学
季刊
1818-0884
辽宁省沈阳市沈河区文化路103号
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76
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