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发表于 2017-7-17 12:49:21
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本帖最后由 shareyuan 于 2017-7-17 12:54 编辑
1. 2010版中國GMP 第二節 生產區 第四十六條
(四)生產某些激素類、細胞毒性類、高活性化學藥品應當使用專用設施(如獨立的空氣凈化系統)和設備;特殊情況下,如採取特別防護措施並經過必要的驗 證,上述藥品制劑則可通過階段性生產方式共用同壹生產設施和設備;
2. PIC/S Part I第3章廠房設施與設備(PREMISES AND EQUIPMENT)--生產區(Production Area)(參見第3章3.6條)
為使因交叉污染所引起之嚴重醫療傷害的風險降到最低,對於一些特殊藥品的生產,例如高致敏性物質(例如:青黴素類)或生物性製劑(例如:來自活的微生物),應有專用且自足圍堵的設施;尚有一些產品,例如某些抗生素、某些荷爾蒙、某些細胞毒類、某些高活性藥物及非藥品的生產不得在同一設施中為之。如採取特別的預防措施,並執行必要的確效時,在例外的情形下,可以接受在同一設施中的時段切換生產原則。工業毒物諸如殺蟲劑及除草劑,不得於藥品之廠房設施中製造
In order to minimize the risk of a serious medical hazard due to cross contamination, dedicated and self-contained facilities must be available for the production of particular medicinal products, such as highly sensitizing materials (e.g. penicillins) or biologicalpreparations (e.g. from live micro-organisms). The production of certain additional products, such as certain antibiotics, certain hormones, certain cytotoxics, and certain highly active drugs andnon-medicinal products should not be conducted in the same facilities. For those products, in exceptional cases, the principle of campaign working in the same facilities can be accepted provided that specific precautions are taken and the necessary validations are made. The manufacture of technical poisons, such as pesticides and herbicides, should not be allowed in premises used for the manufacture of medicinal products.
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