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为使医疗机构的药品质量管理得到提高,进一步完善药品质量的管理体制,对临床用药的安全质量予以保障,就应从药品监管中的药品质量公告作为切入点,进一步加强药品质量公告的作用意义。本文主要对药品质量公告的现状进行研究,对药品质量公告存在问题以及风险监督对策进行分析,着重探究药品质量公告中的改进方式,进而促进药品质量风险监督管理工作的不断完善,推动药品质量得到提升。
In order to improve the quality control of pharmaceuticals in medical institutions, further improve the management system of pharmaceutical quality and ensure the safety and quality of clinical medication, we should take the announcement of quality of medicines in drug supervision as an entry point and further strengthen the significance of the announcement of quality of medicines. This paper mainly studies the status quo of drug quality bulletin, analyzes the existing problems of drug quality bulletin and the risk supervision countermeasures, focuses on the ways to improve the drug quality bulletin, and then promotes the constant improvement of drug quality risk supervision and management to promote the quality of drug Enhance.