| 浅谈制药企业GMP认证后如何巩固和加强质量管理 |
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| 引用本文： | 张红梅.浅谈制药企业GMP认证后如何巩固和加强质量管理[J].医药工程设计,2013(6):31-34. |
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| 作者姓名： | 张红梅 |
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| 作者单位： | 精华制药集团股份有限公司,江苏南通226005 |
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| 摘 要： | 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。
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| 关 键 词： | GMP认证 巩固和加强 质量管理 |
Brief Discussion of How to Consolidate and Strengthen Quality Management in Pharmaceutical Enterprise after GMP Certification |
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| Zhang Hongmei.Brief Discussion of How to Consolidate and Strengthen Quality Management in Pharmaceutical Enterprise after GMP Certification[J].Pharmaceutical Engineering Design,2013(6):31-34. |
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| Authors: | Zhang Hongmei |
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| Institution: | Zhang Hongmei (Jinhua Pharmaceutical Group Share Co., Ltd, Nantong, 226005) |
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| Abstract: | It is not an ending point but starting point for pharmaceutical enterprise to obtain GMP certification. The enterprises should consolidate and strengthen quality management from the aspects of material management, production management and document management. Only in this way, the GMP management in enterprise can be maintained and the enhancement of GMP requirements can be adapted. |
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| Keywords: | GMP certification consolidation and strengthening quality management |
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