洁净室的全球消毒剂标准:提出统一的方法

Tim Sandle
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引用次数: 1

摘要

消毒效果检测是设施污染控制策略的重要组成部分。制药和保健产品设施必须知道,他们使用的产品可以在一系列表面类型上达到有效的微生物杀灭水平。微生物学家和生产管理人员面临的问题是,各种国家和国际标准使用不同的方法。此外,这些标准和方法并不是专门为洁净室编写的,微生物测试板和对数减少期望被认为是不合适的。为了制定适用于所有制药设施洁净室的国际标准,艺康开发了Validex™方法,该方法在本文中进行了独立评估。这种方法包括使用直径2厘米的圆盘,目标是在5分钟内将营养细菌减少3倍;真菌和细菌孢子在10分钟内减少2倍。选择的关键标准和基本原理,以及方法,在本文中提出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A global disinfectant standard for cleanrooms: Presenting a harmonised approach
Disinfectant efficacy testing is an essential part of a facility contamination control strategy. Pharmaceutical and healthcare products facilities must know that the products they are using can achieve effective levels of microbial kill across a range of surface types. The problem faced by microbiologists and production managers is that the various national and international standards use different methodologies. In addition, these standards and methods have not been written specifically for cleanrooms and the microbial test panels and logarithmic reduction expectations are not considered suitable. In order to develop an international standard suitable for all pharmaceutical facility cleanrooms, Ecolab has developed the Validex™ method, which is independently assessed in this paper. This method involves using 2 cm diameter disks, to target a 3 log reduction for vegetative bacteria in 5 minutes; and a 2 log reduction for fungi and bacterial spores in 10 minutes. The key criteria and rationale for selection, along with the methodology, are presented in this paper.
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