In the world of pharmaceutical manufacturing, particularly in the production of Active Pharmaceutical Ingredients (APIs), cleanroom environments are critical. These controlled spaces demand stringent standards to ensure product quality and worker safety. Among these standards, cleanroom lighting plays a pivotal role. This blog explores the key aspects of cleanroom lighting standards for API production.
In environments requiring the utmost sterility - laboratories, hospitals, pharmaceutical plants or electronics factories - even the slightest contamination can lead to serious consequences. Every piece of equipment, including lighting, must meet stringent cleanliness standards.
A cleanroom is an extremely purified region in which temperature the air quality and humidity are kept under strict management. The atmosphere in the cleanroom is filtered to remove other contaminants and dust particles. Cleanrooms are primarily employed for production equipment which is sensitive to contaminants, including hard disk drives, silicon chips, microprocessors and integrated circuits. Cleanroom certification comprises examining the room for assorted parameters, including static electricity, airborne particles, relative humidity, temperature and differential pressure.
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