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06 - 03
DATE
2025
What Is The Difference between ISO And GMP Cleanrooms?
ISO Cleanrooms and GMP Cleanrooms are cleanrooms under two different standards, designed and operated according to ISO standards and GMP specifications respectively.
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05 - 03
DATE
2025
Daily Inspection And Maintenance of Air Shower in Cleanroom
A Cleanroom environment depends heavily on the Air Shower System to maintain its air quality standards. The design of Air Shower Clean Rooms functions as a vital component in all sectors including pharmaceuticals, electronics production and biological research. The longevity of efficient systems depends on routine checks along with regular maintenance.
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04 - 03
DATE
2025
The Importance of Cleanroom Doors
Cleanroom Door is an important part of the Clean Room, applicable to the clean area of the frequent entry and exit of people and the new GMP specification needs to be added to the buffer door of the use. A good Cleanroom Door can tightly seal the space, keep the clean air inside and discharge the polluted air, thus saving a lot of energy.
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12 - 10
DATE
2024
Essential Clean Room Design Principles for Semiconductor Manufacturing: Ensuring Particle-Free Precision
In the high-stakes world of semiconductor manufacturing, precision is not just a goal—it’s a necessity. At the heart of achieving this precision lies the Clean room, an environment meticulously engineered to maintain ultra-low particle levels. As the demand for smaller, faster, and more efficient el
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