2025年3月7日 · GMP stands for Good Manufacturing Practices, a system that ensures that manufactured products—such as food, cosmetics, and pharmaceutical goods—are consistently produced and controlled according to set quality standards. Implementing GMP can help cut losses and waste, and avoid recalls, fines, and jail time.

Good manufacturing practice guidelines provide guidance for manufacturing, testing, and quality assurance in order to ensure that a manufactured product is safe for human consumption or use. Many countries have legislated that manufacturers follow GMP procedures and create their own GMP guidelines that correspond with their legislation.

GMP是英文 GOOD MANUFACTURING PRACTICE 的缩写，中文含义是“良好生产规范”。 世界卫生组织将GMP定义为指导食物、药品、医疗产品生产和质量管理的法规。 GMP是一套适用于制药、食品等行业的强制性标准，要求企业从原料、人员、设施设备、生产过程、包装运输、质量控制等方面按国家有关法规达到卫生质量要求，形成一套可操作的作业规范帮助企业改善企业卫生环境，及时发现生产过程中存在的问题，加以改善。 GMP要求制药、食品等生产企业应具备良好 …

Good Manufacturing Practices (GMP, also referred to as 'cGMP' or 'current Good Manufacturing Practice') is the aspect of quality assurance that ensures that medicinal products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the product specification.

GMP是Good Manufacturing Practice的简称，即药品生产质量管理规范。 检查对象是：①人；②生产环境；③制剂生产的全过程。 "人"是实行GMP管理的软件，也是关键管理对象，而"物"是GMP管理的硬件，是必要条件，缺一不可。

《药品生产质量管理规范》（Good Manufacturing Practice of Medical Products，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，是提高药品质量的重要措施。 世界卫生组织，60年代中开始组织制订药品GMP，中国则从80年代开始推行。 1988年颁布了中国的药品GMP，并于1992年作了第一次修订。 十几 …

is designed for staff of National Control Au- thorities and selected vaccine manufacturers meeting specific entrance criteria. This document is designed for use by participants in the Global Training Network, specifically for those participating in curricula re- lated to Good Manufacturing Practices.

GMP认证 的基本概念和要求. GMP（Good Manufacturing Practice）即良好生产规范，是一套适用于制药、食品等行业的强制性标准，旨在确保产品从原料采购、人员培训、设施设备、生产过程、包装运输到质量控制等各个环节符合国家卫生质量要求。

GMP是Good Manufacturing Practice的縮寫，中譯是「良好作業規範」或「優良製造標準」的意思，是特別注重產品在製造過程中之品質及衛生安全的自主性管理制度。

2015年11月20日 · Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be …