In a pharmaceutical sense, a clean room refers to a room that complies with GMP (Good Manufacture Practice of Medical Products, GMP) aseptic specifications. Due to the strict requirements of the production environment for the upgrading of manufacturing technology, clean laboratories are also known as the "patron saint of high-end manufacturing."
A clean room, also known as a clean room, is usually used as part of professional industrial production or scientific research, including the manufacture of pharmaceuticals, integrated circuits, CRT, LCD, OLED and microLED displays, etc. Cleanrooms are designed to maintain extremely low levels of particulates such as dust, airborne organisms, or vaporized particles. Rather, a cleanroom has a controlled contamination level specified by the number of particles per cubic meter at a specified particle size. A clean room can also refer to any given containment space in which settings are made to reduce particulate contamination and control other environmental parameters such as temperature, humidity, and pressure.
In the pharmaceutical sense, a clean room refers to a room that complies with the requirements of the GMP regulations defined in the GMP aseptic regulations (i.e. EU and PIC/S GMP Guidelines Annex 1 and other standards and guidelines required by the local health authority), and is the conversion of ordinary rooms The combination of engineering design, fabrication, finishing and operational control (control strategy) required for a cleanroom.
Many industries will use clean rooms, as long as there are small particles that will adversely affect the production process, there will be clean rooms. They vary in size and complexity and are widely used in industries such as semiconductor manufacturing, pharmaceuticals, biotechnology, medical devices, and life sciences, as well as critical process manufacturing commonly found in aerospace, optics, military, and the Department of Energy.
