摘要
目的帮助药品生产企业充分认识药品不良反应监测工作的意义及其在监测工作中的主体地位。方法从国内对药品生产企业的相关法规要求的基础上分析了国内药品生产企业在药品不良反应报告与监测的现状及存在的问题,提出了我国药品生产企业如何开展和落实药品不良反应报告和监测工作的相关建议。结果与结论药品生产企业应当进一步加强对药品不良反应监测与报告的认识和理解,构建全面的质量管理体系,设置专门的机构和人员负责药品不良反应监测工作,并加强企业内部的培训宣传工作,积极落实企业作为"药品安全第一责任人"的责任。
Objective To help drug manufacturers to understand and recognize the significance and their dominant position in the adverse drug reaction （ADR） monitoring work. Methods Based on the analysis of relevant regulations, the problems of the domestic drug manufacturers in ADR reporting and monitoring were analyzed, and related suggestions on how to develop and implement ADR reporting and monitoring were put forward. Results and Conclusion Drug manufacturers should strengthen their cognition and understanding of ADR monitoring and reporting, structure the quality management system, set up expert organizations and full-time personnel responsible for ADR monitoring. At the same time, drug manufacturers should strengthen their internal training to commit the responsibility of ＂drug safety first person＂ actively.
出处
《中国药物警戒》
2016年第3期159-161,共3页
Chinese Journal of Pharmacovigilance
关键词
药品生产企业
药品上市后研究
第一责任人
drug manufacturer
post-marketing study
the first person responsible
