摘要
质量高的药品是经过生产的,与检测无较大关系,为了有效控制药品的质量,维护人体的用药安全,需要对整个药品生产过程进行控制。但是,在具体生产期间还存在一些问题,如违反工艺规程。所以,监管部门要加强对工作的重视。
High quality drugs are produced,which has nothing to do with detection.In order to effectively control the quality of drugs and maintain the safety of drug use,the whole drug production process needs to be controlled.However,there are still some problems in the specific production period,such as violation of process regulations.Therefore,the regulatory authorities should pay more attention to the work.
出处
《科技创新与应用》
2020年第16期183-184,共2页
Technology Innovation and Application
关键词
药品
生产工艺
规程
监管
drugs
production process
procedures
supervision