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各相关单位:为推进实施《药品不良反应报告和监测管理办法》,有效开展药品不良反应监测和上市后再评价工作,国家食品药品监督管理总局药品评价中心、国家食品药品监督管理总局高级研修学院、《中国药物警戒》编辑部定于2014年9月在江苏举办药品上市后风险管理技术实践培训班。本次培训班主要涉及法规与技术指南解读、药品上市后研究与再评价、国内外药品风险管理的理论与实践的三大模块,为从事药品风险管理的相关人员提供学习和交流机会。现将有关事项通知如下:
Relevant units: In order to promote the implementation of “Adverse Drug Reaction Reporting and Monitoring Management Measures”, effectively carry out drug adverse reaction monitoring and re-evaluation after listing, the State Food and Drug Administration Drug Evaluation Center, the State Food and Drug Administration Advanced Training Institute The Editorial Department of “China Pharmacovigilance” is scheduled to hold a hands-on training course on risk management after drug listing in Jiangsu Province in September 2014. The course mainly covers three modules of the interpretation of laws and regulations, the research and revaluation after the drug listing, the theory and practice of drug risk management both at home and abroad, and provides opportunities for learning and exchange for those involved in drug risk management. The relevant matters are hereby notified as follows: