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Customized Modular ISO Clean Rooms

Categories ISO Clean Rooms
Brand Name: alphaclean
Model Number: customized
Certification: ce
Place of Origin: china
MOQ: 1 set
Price: negotiation
Payment Terms: L/C, T/T
Delivery Time: 20 days
Packaging Details: Polywood packing
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
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    • Product Details
    • Company Profile

    Customized Modular ISO Clean Rooms

    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
    50-60
    >10Pa
    10-30%
    Class 10000
    15-25
    >10Pa
    Class 100000
    10-15
    >10Pa

    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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