| Customization: | Available |
|---|---|
| Application: | Pharmaceutical;Laboratory;Electronics |
| Clean Grade: | ISO5/6/7/8 |
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Audited Supplier Audited by an independent third-party inspection agency
| Cleanliness | Class 100 to Class 100000, ISO 5 to ISO 8, Class B to Class D |
| Project include | 1. Structure: Wall Panel, Ceiling Panel, Windows, Doors, Various Fittings, Flooring |
| 2.Electric: Lighting, Switch, Cables, Wires, Power Distribution Cabinet, etc | |
| 3.HVAC: AHU, Ducting, Piping, Chiller, dehumidifier, etc. | |
| 4.Auto-control: PLC Controller, Sensors for Humidity and Temperature, Control Panel | |
| 5. Process Piping System: Gas, Water Pipeline | |
| Temperature&Humidity | As clients request |
| Application | Pharmaceutical Industry |
| Qualification Documents | IQ, OQ, PQ,DQ |
| Our Service |
Professional Consultation, User-friendly English Sofaware, 24 hours technical support, |
This is a clean room full service construction under GMP request. Turnkey project.
A Cleanroom or clean room is an environment, typically used in manufacturing or scientific research, that has a
low level of environmental pollutants such as dust, airborne microbes, aerosol particles and chemical vapors.
More accurately, a cleanroom has a controlled level of contaimination that is specified by the number of particles
per cubic meter at a specified particle size.
To give perspective, the ambient air outside in a typical urban environment contains 35,000,000 particles per cubic
meter in the size range 0.5um and larger in diameter, corresponding to an ISO9 cleanroom, while an ISO clean
room allows no particles in that size range and only 12 particles per cubic meter of 0.3um and smaller.
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