In the medicinal sense, the clean room is the GMP sterile specification clean room. Clean laboratories, due to the strict requirements of manufacturing technology upgrading, are also known as the “guardian of high – end manufacturing”.
Clean room is designed to maintain extremely low levels of particles such as dust, organisms in the air, or vaporized.
The clean room has a controlled level of pollution, defined by the number of particles per cubic meter at the specified particle size.
Clean room may also refer to any given accommodation space in which to reduce particulate pollution and control other environmental parameters such as temperature, humidity and pressure.
In the medicinal sense, a clean room is a room that meets the requirements of the GMP specifications as defined in the GMP Sterity Specification, and is a combination of engineering, manufacturing, completion, and operational control (control strategy) required to convert a common room into a clean room.
Many industries will use dust – free clean rooms, in places where small particles will adversely impact on the production process. They vary in size and complexity and are widely used in semiconductor manufacturing, pharmaceutical, biotechnology, medical equipment and life sciences, as well as key process manufacturing common in the Ministry of Aerospace, Optics, Military and Energy.
