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药品检验是按照法定的药品标准对药品的真伪及其质量优劣进行检定的学科。在药品检验过程中,会遇到各种各样的矛盾和问题,要分析和处理好这些矛盾和问题,就要求我们必须坚持从实际出发,坚持实事求是的基本原则,按药品检验客观规律办事,而不能从主观愿望出发,从上级指示出发,凭书本原则和经验办事。本文就药品的标准制订、检验过程、检验报告等环节作一论述。 一、药品标准的制订要源于实际 人们对药品所制订的标准就是对药品质量
Drug testing is in accordance with the statutory drug standards on the authenticity of medicines and their quality advantages and disadvantages of the test subjects. In the process of drug inspection, we will encounter various contradictions and problems. To analyze and handle these contradictions and problems requires us to adhere to the basic principle of seeking truth from facts and acting in accordance with the objective laws of drug inspection based on reality, But not from the subjective desire to proceed from the instructions of the higher authorities, with the book principles and experience work. This article on the standard drug formulation, testing process, inspection reports and other links to make a discussion. First, the formulation of drug standards from the actual people of the standard set by the drug is the quality of the drug