药品管理法律制度如何顺应医药产品创新、市场化程度提升、市场主体变化以及政府监管手段和措施的更新,本文根据药品管理实践对法律制度变革的需求,列举药品上市后监管制度相关的14个议题,研究梳理了实践中存在的问题以及下一步法律制度修改的意见和建议。
<<How could the medicine administration law system be adapted to innovative medical products,increased marketization degree,changed market entities,and updated regulatory means and measures?According to the demands for the legal system reform in medicine management practices,the author in this paper listed 14 topics related to the post-marketing medicine supervision system,studied and summarized the problems in practice,and gave opinions on and suggestions for modifying the legal system in the next step.
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