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制药企业通过GMP认证,绝对不是一个终点,而是一个新的起点,更要从物料管理、生产管理、文件管理等各个方面,巩固和加强质量管理。只有这样,才能保持和发展企业的GMP管理水平,以适应不断提升的GMP要求。
GMP certification by the pharmaceutical companies, is definitely not an end, but a new starting point, but also from the material management, production management, document management and other aspects to consolidate and strengthen quality management. The only way to maintain and develop the GMP management of enterprises to meet the ever-increasing GMP requirements.