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过去人们对药品质量,总认为只要经过检验符合药典规定就是好的,其实这很不全面,也不完全正确,因为如果不符合优良生产和质量管理规范就不可能保证每一批号药品均匀、优质,仍然有混药或有害杂质存在的可能,何况医疗单位较生产单位复杂得多。一、药品质量管理的概念
In the past, people always considered the quality of medicines as long as they were tested and found to be in compliance with the Pharmacopoeia. In fact, this is not comprehensive and not entirely correct because it is impossible to ensure that every batch of medicines is uniform and of good quality if it does not meet the requirements of good production and quality control , There is still the possibility of mixed drugs or harmful impurities, not to mention that the medical units are much more complicated than the production units. First, the concept of drug quality management