医药工业洁净厂房室内悬浮粒子检测方法概述  

Introduction forTestMethod of Airborne Particles In Pharmaceutical Industry Clean Room

作　　者：牛勇 Niu Yong(Lanzhou Institute of Biological Products Co.,Ltd Lanzhou,Gansu,730046)

机构地区：[1]兰州生物制品研究所有限责任公司,甘肃兰州730046

出　　处：《科学与信息化》2020年第30期124-125,共2页Technology and Information

摘　　要：医药工业洁净厂房采用粒子计数器,通过对单位体积空气中特定粒径悬浮粒子数量的测定,确定洁净室洁净度级别。本文介绍了医药工业洁净厂房室内悬浮粒子的检测方法,重点对测试条件、悬浮粒子采样、数据计算、结果判定、注意事项等进行了介绍,以便于确定洁净室洁净度是否达到GMP规范要求,满足生产需要。The pharmaceuticalindustryclean room uses particle counter to determine air cleanliness of cleanroom by measuring the number of airborne particle in specific volume of air in unit volume.This paper introduces the detection method of airborne particles in pharmaceutical clean room,focusing on the test conditions,airborne particles sampling,data calculation,result judgment,matters needing attention,etc.,so as to determine whether the air cleanliness achieve the GMP standard and meet the production needs.

关 键 词：医药洁净室 悬浮粒子检测 GMP 

分 类 号：TU8[建筑科学]