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作 者:谭云 TAN Yun(Shanghai Pharmaceutical Co.,Ltd.,Shanghai 200032,China)
机构地区:[1]上药控股有限公司,上海200032
出 处:《上海医药》2022年第9期47-49,57,共4页Shanghai Medical & Pharmaceutical Journal
摘 要:通过陈述现行法律法规中无过错责任界定的法理依据、分析药品经营、使用环节中减免责条款使用现状,明确药品经营企业、使用单位的责任范围,同时明确梳理出其可以依法予以免责或者减轻处罚的具体情形,探索新《中华人民共和国药品管理法》施行中具有可操作性的细则,为药品事中事后监管积极探索可行性方案。By stating the legal basis for the definition of the no-fault liability in current laws and regulations,analyzing the current situation of the use of the exemption clause in the process of drug distribution and usage,the scope of responsibility of drug trading enterprises and user units is clarified.According to the law,the specific circumstances in which they can be exempted from liability or mitigated punishment are sorted out.Moreover,the operable rules in the implementation of the new Drug Administration Law are explored to figure out a feasible scheme for the supervision of drugs during and after the event.
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