Achieving optimal sterility and product quality in sensitive manufacturing environments necessitates precise control over particulate contamination. This is where cleanroom classification comes into play, establishing standardized guidelines to quantify the level of air purity within a controlled space. The ISO (International Organization for Stand… Read More

Robust design qualification (DQ) is a essential step in establishing the suitability of a cleanroom for its intended application. This thorough process involves a systematic analysis of the cleanroom's design to ensure it meets all relevant requirements and standards. DQ activities typically comprise reviews of engineering drawings, simulations, an… Read More