Automated Systems and automated processes are rapidly transforming the conduct of sterile room activities. Historically , these spaces relied heavily on human labor, which created issues relating to contamination control and productivity . Now, robotic platforms are allowing enhanced consistency

Robust design qualification (DQ) is a fundamental step in establishing the suitability of a cleanroom for its intended use. This rigorous process involves a systematic evaluation of the cleanroom's configuration to ensure it meets all relevant requirements and standards. DQ steps typically includ