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中国药典1977年版已对一部分稳定性较差的药品制定了有效期限,这对于保证药品的安全有效大有好处。除此之外。我认为其它一些药品也应根据其性质、目前国内一般的生产水平及储存条件,制订一个统一的药厂对药品质量的负责期限。药厂对药品质量的负责期限,系指药品出厂后药厂对其药品质量的负责期限。它既不是药品的有效期,也不是药品的贮存期、超过负责期限仍为合格品时仍可继续使用。制订药厂对药品质量的负责期限可以进一步加强药品生产的质量管理,促进生产单位努力提高药品质量和包装质
The Chinese Pharmacopoeia 1977 edition has set a period of validity for some of the less stable drugs, which is of great benefit to ensure the safety and effectiveness of the drug. In addition. I think some other drugs should also be responsible for formulating a unified pharmaceutical product liability deadline for the quality of the drug according to its nature, the current general domestic production level and storage conditions. The responsibility of the pharmaceutical manufacturer for the quality of the drug refers to the period in which the pharmaceutical manufacturer is responsible for the quality of the drug after the drug is manufactured. It is neither the validity of the drug nor the shelf life of the drug, but it can still be used beyond the time limit of responsibility. The formulation of the responsibility of the pharmaceutical manufacturer for the quality of pharmaceutical products can further enhance the quality control of pharmaceutical production and promote the efforts of production units to improve the quality and quality of pharmaceutical products