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GMP Sterile Aseptic ISO Laboratory Clean Rooms Physical Chemical

    Buy cheap GMP Sterile Aseptic ISO Laboratory Clean Rooms Physical Chemical from wholesalers
     
    Buy cheap GMP Sterile Aseptic ISO Laboratory Clean Rooms Physical Chemical from wholesalers
    • Buy cheap GMP Sterile Aseptic ISO Laboratory Clean Rooms Physical Chemical from wholesalers
    • Buy cheap GMP Sterile Aseptic ISO Laboratory Clean Rooms Physical Chemical from wholesalers

    GMP Sterile Aseptic ISO Laboratory Clean Rooms Physical Chemical

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    Brand Name : alphaclean
    Model Number : ISO clean room
    Certification : ce
    Price : negotiation
    Payment Terms : L/C, T/T, Western Union
    Delivery Time : 20 days
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    GMP Sterile Aseptic ISO Laboratory Clean Rooms Physical Chemical

    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.


    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

    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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