In an Electronic Cleanroom, the gray zone, as a special area, plays a crucial role. It not only physically connects the clean area with the non-clean area, but also functionally plays the role of buffer, transition and protection.
Purification engineering specially designed room, regardless of how the external air conditions change, the room has to maintain the original set requirements of cleanliness, temperature and humidity, and pressure and other properties.
ISO Cleanrooms and GMP Cleanrooms are cleanrooms under two different standards, designed and operated according to ISO standards and GMP specifications respectively.
The semiconductor industry together with biomedical and food processing require Cleanrooms to guarantee product quality. Cleanroom management follows the international requirements described in the ISO 14644 standard that details air cleanliness classes and test procedures and compliance protocols.
Amber is a professional engaged in providing turnkey solution in a clean room project such as hospital operating room, ICU, ward, pharmaceutical, bio-lab and so on.
