화학공학소재연구정보센터
Kunststoffe-Plast Europe, Vol.91, No.5, 58-58, 2001
Guidelines for demonstrating standardised suitability for cleanroom operation
To market products for pharmaceutical or medical purposes worldwide, it is not sufficient simply to manufacture them under cleanroom conditions. It is also necessary to demonstrate that all the machines and equipment used are suitable for cleanroom operation - a process known as qualification.