In the context of the continuous development of high-precision, miniaturised electronic products, the electronic manufacturing industry has increasingly stringent requirements for the cleanliness of production environments. Electronic Cleanrooms not only affect product yield rates, but also directly impact the reliability and performance of products such as chips, sensors, and LEDs. This article will outline the common grade requirements for electronic manufacturing cleanrooms and the corresponding cleanroom equipment standards.
 

A Clean Room is a specially designed workshop that removes micro-particles, harmful air, bacteria and other pollutants from the air within a certain space, and controls the indoor temperature, cleanliness, indoor pressure, airflow velocity and distribution, noise and vibration, lighting, and static electricity within a certain range of requirements. In other words, regardless of changes in external air conditions, the indoor environment can maintain the originally set requirements for cleanliness, temperature, humidity and pressure.

The efficacy of medicines is to cure diseases and save lives, which also determines the special nature of medicine production. ‘Medicine quality is designed and produced,’ and the production environment that ensures medicine quality is also being improved accordingly. So how much does it cost to build a Clean Room for medicines?

In the sterile rooms of pharmaceutical factories, the precision production lines of semiconductor chips, and even in biological laboratories, high-efficiency filters are the soul of maintaining a clean environment. Especially when used with HEPA Box and HEPA Filter Unit, they are called the 'heart and lung system' of the cleanroom.