Pharmaceutical Industry Background In sterile drug production, compressed air systems directly contact APIs (Active Pharmaceutical Ingredients), primary packaging, and filling equipment. Contaminants as small as 0.1μm particles or 0.01mg/m³ oil residues can compromise product sterility, triggering FDA 483 observations. Globally, 25% of pharmaceutical recalls (2023 WHO report) link to compressed air contamination. Why Pharmaceutical Manufacturing […]