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随着现代社会经济的发展,我国医学水平也在不断提高,并且医药行业已经成为了现代医学领域的主要发展分支,再加上当今社会科技与经济的不断进步之下,医学领域国际交流学习越来越频繁,对于医药种类也在不断改变和增加之中,由于健康是人类生存和生活的首要标准,可以说对医药试剂的应用是否合理直接关系到了人类生命的安全性,尤其是西药试剂,在当今社会的情况下,对药物高水平高成效的需求也愈来愈高,与此同时我们对用于临床上西药试剂的质量和性能也提出了更高的要求,为了能够在确保人们健康安全性的情况下不减少医药业私人利益和企业效益,如何根据西药药剂自身的特点和不同的类别,来利用相应的监督管理措施规范医药制剂的应用成为这篇文章研究的主要课题。
With the development of modern society and economy, the medical level of our country is also constantly improving, and the pharmaceutical industry has become a major development branch in the field of modern medicine. Coupled with the continuous improvement of social science and technology and economy, the international exchange and study in the field of medicine More and more frequent, for the type of medicine is also constantly changing and increasing, as health is the primary standard of human existence and life, it can be said that the application of medical reagents is directly related to the safety of human life, especially the Western medicine, In today’s society, the demand for high-level and high-effect drugs is getting higher and higher. Meanwhile, we also put higher requirements on the quality and performance of clinical western medicine reagents. In order to ensure people’s health How to regulate the application of pharmaceutical preparations according to the characteristics and different categories of western medicine and its corresponding supervision and management measures has become the main topic of this article research without reducing the private benefits and business benefits of the pharmaceutical industry in the case of safety.