论文部分内容阅读
药品标准是国家对药品的质量规格和检验方法所做的技术规定。《中华人民共和国药品管理法》第二十三条规定:“国务院卫生行政部门颁布的《中华人民共和国药典》和药品标准为国家药品标准”。据卫生部“关于颁布《中华人民共和国药典》一九八五年版的通知”,1985年版(以下简称85版)中国药典已于1986年4月1日正式执行。下面就85年版药典一部做一简单介绍。一、《中华人民共和国药典》的修订概况
Drug standards are the technical regulations of the country for the quality specifications and test methods of drugs. Article 23 of the “People’s Republic of China Drug Administration Law” stipulates: “The ”Pharmacopoeia of the People’s Republic of China“ and drug standards promulgated by the State Council’s administrative department of health shall be national drug standards.” According to the “Notice on the Promulgation of the 1985 Edition of the Pharmacopoeia of the People’s Republic of China” of the Ministry of Health, the 1985 edition (hereinafter referred to as the 85 edition) of the Chinese Pharmacopoeia was formally implemented on April 1, 1986. The following is a brief introduction to the 85th edition of the Pharmacopoeia. I. Overview of the Amendment to the Pharmacopoeia