Airborne particulates pose a significant risk to controlled environments, particularly in medical device and pharmaceutical manufacturing. These microscopic contaminants originate from various sources, including personnel, equipment, raw materials, and even the structural components of the facility itself. While dust is one of the most common particulate types, cleanrooms also face risks from fibers, microbial contaminants, and chemical residues.
In medical manufacturing, contamination control is a critical factor in ensuring product safety and regulatory compliance. Unlike technology manufacturing, where particulate contamination can impact product functionality, medical cleanrooms must prioritize sterility to mitigate health risks associated with microbial contamination. Without stringent control measures, airborne particulates can compromise the quality of medical products, leading to safety concerns and regulatory violations.