Alpha Clean Air Technology Co.,Ltd
| Payment Terms | L/C, T/T, Western Union |
| Delivery Time | 20 days |
| Packaging Details | Polywood packing |
| clean room level | ISO 5 - 8 |
| main material | wall panels, window, door |
| Application | pharma,electronics,lab ,food, hospital |
| scope | struture , HVAC , electricity / monitoring |
| period | 1 - 4 months |
| service | field installation , commissioning and training,engineer are able to service machinery overseas |
| warranty | 1 year |
| document | verification and certification |
| Brand Name | alphaclean |
| Model Number | ISO clean room |
| Certification | ce |
| Place of Origin | china |
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Product Specification
| Payment Terms | L/C, T/T, Western Union | Delivery Time | 20 days |
| Packaging Details | Polywood packing | clean room level | ISO 5 - 8 |
| main material | wall panels, window, door | Application | pharma,electronics,lab ,food, hospital |
| scope | struture , HVAC , electricity / monitoring | period | 1 - 4 months |
| service | field installation , commissioning and training,engineer are able to service machinery overseas | warranty | 1 year |
| document | verification and certification | Brand Name | alphaclean |
| Model Number | ISO clean room | Certification | ce |
| Place of Origin | china | ||
| High Light | Aseptic ISO Clean Rooms ，ISO 7 Class 10000 Clean Room ，Aseptic Laboratory Clean Rooms | ||
GMP Sterile Aseptic ISO Clean Rooms Physical Chemical Laboratories
GMP Sterile Clean Aseptic Laboratory
Non-sterile areas are generally equipped with physical and chemical laboratories and research and development laboratories.
PCR gene amplification laboratory is again not discussed, its layout solidified, rigorous.
Conventional quality control area for GMP field, and the production area, storage area, office area, water and electrical power area constitute a common GMP factory (pharmaceutical factory, medical equipment factory, food factory, cosmetics factory, etc.).
The conventional quality control area includes sterile experimental area, sampling room, physical and chemical laboratory, and research and development laboratory.
Most factories of the sterile area commonly divided into non-clean area preparation room and Class10000 positive control room, class 10000 sterility test room, class 10000 microbial limit test room, and personal clean auxiliary room (hand washing, wear Sterile clothes, hand-buffering, laundry, sanitary ware, stationware washing).
In the three class 10,000 (2013 new GMP C grade) rooms, relative negative pressure on the other two rooms in the positive control room , 100%independent fresh air conditioning and exhausted after high efficiency filtered;
Three laboratories are equipped with ultra-clean benches.
Party A shall decide whether to use the biosafety cabinet between positive controls, and there is no mandatory requirement in the current standard.
Temperature requirements: 22 + 2 ℃,
Humidity RH = 45% ~ 65%; This is different from the low-level production area (18 ~ 28 ℃);
Is the constant temperature and humidity air conditioner used?
Depends on the country area
Company Details
Business Type:
Manufacturer
Year Established:
2015
Total Annual:
200000-400000
Employee Number:
50~100
Ecer Certification：
Verified Supplier
Alpha clean air technology co ltd is a Cleanroom Turnkey Solution provider specializing in design,manufacturing,construction,commissioning and validation services of cleanrooms and associated products. The company is located in the Shenzhen Guangdong Province, The company has established a t... Alpha clean air technology co ltd is a Cleanroom Turnkey Solution provider specializing in design,manufacturing,construction,commissioning and validation services of cleanrooms and associated products. The company is located in the Shenzhen Guangdong Province, The company has established a t...
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