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根据《中华人民共和国药品管理法》的规定和卫生部、国家医药管理局的统一部署,上海市卫生局和上海市医药管理局在1994年联合组织开展了全市药品生产、经营企业换发“药品生产、经营企业合格证”和“药品生产、经营企业许可证”以及医院换发“制剂生产许可证”工作。这项工作大致进行了四个阶段。 一、计划筹备阶段 按照《药品管理法》的规定,“两证”的审核、换发每五年进行一次。
In accordance with the provisions of the “Drug Administration Law of the People’s Republic of China” and the unified arrangements of the Ministry of Health and the State Pharmaceutical Administration, the Shanghai Municipal Bureau of Health and the Shanghai Municipal Bureau of Medical Administration jointly organized in 1994 the city’s pharmaceutical production and business enterprises to renew their “Drugs Production and operation of corporate certification ”and“ drug production and business license ”and the hospital renewal“ preparation production license ”work. This work has been basically carried out in four stages. First, the planning stage of preparation In accordance with the “Drug Administration Law”, “two cards” review, renewal every five years.