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药品的质量控制是药品生产企业及政府主管机构的重要研究课题。药品质量受医药企业生产、检测水平影响,并受政府监管机构严格把关。针对我国药品生产监管现状进行分析,药企应加强药品生产过程质量控制,规范药品检测标准;政府机构应明确部门职责;结合国外先进管理经验,重视药品管理过程中公众参与度,推动社会共治的药品管理格局,将有利于维护我国药品安全。
Quality control of pharmaceutical products is an important research topic for pharmaceutical manufacturers and government agencies. The quality of medicines is affected by the production and testing levels of pharmaceutical enterprises and is strictly controlled by the government regulatory agencies. According to the analysis of the status quo of drug production supervision in our country, the pharmaceutical enterprises should strengthen the quality control of the drug production process and standardize the drug testing standards; the government agencies should clarify the departmental responsibilities; combine the advanced foreign management experience with the public participation in the drug management process and the promotion of social co-governance The pattern of drug administration will help maintain the safety of our medicines.