世界卫生组织HVAC非无菌制药指南WHO-937

WHO 937 Annex 附件 2Supplementary guidelines on good manufacturing practices for heating, ventilation and air-conditioning systems for non-sterile pharmaceutical dosage forms在 GMP 的基础上补充指导药剂生产的供暖，通风，空调系统的指导条例。1. Introduction 介绍2. Scope of document 文本范围3. Glossary 术语表4. Protection 保护4.1 Products and personnel 产品和人员4.2 Air filtration 空气过滤4.3 Unidirectional airflow 单向空气流4.4 Infiltration 渗透4.5 Cross-contamination 交叉污染4.6 Temperature and relative humidity 温度和相对湿度5. Dust control 固体颗粒污染物控制6. Protection of the environment 环境保护6.1 Dust in exhaust air 排气中的固体颗粒6.2 Fume removal 烟尘的祛除7. Systems and components 系统和构造7.1 General 概论7.2 Recirculation system 循环系统7.3 Full fresh air systems 送风系统8. Commissioning, qualification and maintenance 运转，资格和维护8.1 Commissioning 运转8.2 Qualification 资格8.3 Maintenance 维护References 文献451. Introduction 介绍Heating, ventilation and air-conditioning (HVAC) play an important role in ensuring the manufacture of quality pharmaceutical products. A well designed HVAC system will also provide comfortable conditions for operators.加热，通风，空调（HVAC）系统在保证药品质量的生产上起着至关重要的作用。同时，设计完善的系统也会给操作人员提供舒适的工作环境。These guidelines mainly focus on recommendations for systems for manufacturers of solid dosage forms. The guidelines also refer to other systems or components which are not relevant to solid dosage form manufacturing plants, but which may assist in providing a comparison between the requirements for solid dosage-form plants and other systems.这些条例主要是针对固体药剂生产车间而提出的。但同时在涉及到与固体药剂生产无关的其它生产中，这些条例可以比较固体药剂生产车间和其它车间生产规格上的具体要求。HVAC system design infl...