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GMP即药品生产管理规范。它包括了硬件(厂房,机械、设备等)及软件(规章制度、文件、卫生及人员训练等)两部分。药学系主任郑梁元同志于6月5日在南京药学院药厂礼堂作了赴日考察GMP执行情况的报告。重点介绍了日本卫材和佐藤两公司所属5个药厂的GMP执行情况,共分四个方面:1.严密制造卫生包括厂址选择、厂房设计、清洁卫生及职工训练。2.严格控制质量包括核对制度,原材料、中间体、半成品及成品检查制度,留样检查制度等。
GMP is the pharmaceutical production and management practices. It includes hardware (plant, machinery, equipment, etc.) and software (rules and regulations, documentation, health and personnel training, etc.) in two parts. On June 5, Comrade Zheng Liangyuan, director of the department of pharmacy, made a report on the implementation of GMP in Japan at the pharmaceutical factory auditorium of Nanjing Pharmaceutical College. It mainly introduces the implementation of GMP of 5 pharmaceutical companies owned by Japan Eisai and Sato. It is divided into four aspects: 1. Strict hygiene includes site selection, plant design, sanitation and staff training. 2. Strict control of quality, including the verification system, raw materials, intermediates, semi-finished products and finished product inspection system, sample-like inspection system.