《药品生产质量管理规范》(1998年修订)于1999年8月1日起施行。药品ＧＭＰ是药品生产和质量管理的基本准则,适用于药品制剂生产的全过程和原料药生产中影响成品质量的关键工序。大力推行药品ＧＭＰ,是为了最大限度地避免药品生产过程中的污染和交叉污染,降低各种差错的发生,是 The “Code of Practice for the Quality Control of Pharmaceutical Production” (revised in 1998) came into effect on August 1, 1999. Drugs GMP is a basic guideline for pharmaceutical production and quality control and is applicable to the key processes affecting the quality of finished products in the whole production process of pharmaceutical preparations and in the production of pharmaceutical raw materials. Vigorously promote the drug GMP, is to maximize the avoidance of pollution in the pharmaceutical production process and cross-contamination and reduce the occurrence of various errors is