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Alpha Clean Air Technology Co.,Ltd

Customized Modular ISO Clean Rooms

Product Details:
Place of Origin: china
Brand Name: alphaclean
Certification: ce
Model Number: customized
Payment & Shipping Terms:
Minimum Order Quantity: 1 set
Price: negotiation
Packaging Details: Polywood packing
Delivery Time: 20 days
Payment Terms: L/C, T/T
  • Detail Information
  • Product Description

Detail Information

Application: Pharmaceutical,electronics,lab,food,hospitals Production Time: 1 Month
Services: Field Installation , Commissioning And Training,engineer Are Able To Service Machinery Overseas Clean Room Structure: Ceiling And Wall Panels, Flooring, Air Conditioner,air Filter System
Clean Level: ISO 5, 6, 7, 8, 9,10 Airflow: 2000 - 50000 M3/h
HVAC: Air Handling Unit Optional Filter Stage: G4 + F7 +H10 + H13
High Light:

Customized Modular ISO Clean Rooms


GMP Sterile ISO Clean Rooms


GMP Sterile Clean Room Lab

Product Description

Customized Modular ISO Clean Rooms


Customized modular clean room GMP sterile cleaning laboratory


General Class Level
Air exchange times
Relative Static Pressure
New Air Percentage
Class 1000
Class 10000
Class 100000


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

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