At Pharma United Co., Ltd, our expert staff has 16 years of cleanroom experience. We will design, manufacture and install a custom cleanroom based on your requirement.
Item No :
Cleanroom General ContractorProduct Origin :
ChinaShipping Port :
ShanghaiCleanroom level standards
Cleanrooms often use the maximum allowable particle count per cubic foot or cubic meter specified by the US Federal S209E standard and ISO 14644-1 standard to determine the cleanliness level.
| Maximum allowable amount of fine dust particles of various sizes | |||||||||||||
| 0.1μm | 0.2μm | 0.3μm | 0.5μm | 1μm | 5μm | ||||||||
| US F.S209E | ISO14644-1 | (m3) | (ft3) | (m3) | (ft3) | (m3) | (ft3) | (m3) | (ft3) | (m3) | (ft3) | (m3) | (ft3) |
| ISO1 | 10 | 2 | 0 | 0 | 0 | 0 | |||||||
| ISO2 | 100 | 24 | 10 | 4 | 0 | 0 | |||||||
| C-1 | ISO3 | 1000 | 35 | 237 | 8 | 102 | 3 | 35 | 1 | 8 | 0 | 0 | 0 |
| C-10 | ISO4 | 10000 | 350 | 2370 | 75 | 1020 | 30 | 352 | 10 | 83 | 2 | 0 | 0 |
| C-100 | ISO5 | 100000 | 3500 | 23700 | 750 | 10200 | 300 | 3520 | 100 | 832 | 24 | 29 | 0 |
| C-1K | ISO6 | 1000000 | 35000 | 237000 | 7500 | 102000 | 3000 | 35200 | 1000 | 8320 | 236 | 293 | 7 |
| C-10K | ISO7 | 352000 | 10000 | 83200 | 2360 | 2930 | 70 | ||||||
| C-100K | ISO8 | 3520000 | 100000 | 832000 | 23600 | 29300 | 700 | ||||||
A: When a customer hires a design build cleanroom company to handle design, manufacturing, cleanroom, cleanroom filtration, electrical, AC, cleanroom flooring, and cleanroom certification.
A: The benefits are a better cleanroom design, faster installation, less change orders, and single responsible party – the modular design build cleanroom company. When you hire Pharma United Co., Ltd, you get 18 years of experience and expertise designing and assembling turnkey cleanrooms.
A: Typically, turnkey cleanrooms are built by Pharma United who have design build business model. While they typically use local subcontractors to install cleanroom HVAC, electrical wiring and flooring, they coordinate closely with filtration assembly to enable the faster assembly times and superior performance.
A: Large cleanroom projects, cleanrooms with very tight temperature and RH specification, ISO5 and ISO6 cleanrooms benefit the most from turnkey cleanroom approach.
A: Yes. Pharmaceutical and medical devices cleanrooms are typically a key part of the FDA validation process so ensuring the cleanroom meets the technical requirements is an ideal match for turnkey cleanroom process.
A: The most common problem in non turnkey cleanrooms is the AC does not keep the cleanroom cool. Other problems with non turnkey cleanrooms often include unexpected change orders and significantly longer cleanroom installation time.
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