

Add to Cart
Customized Modular ISO Clean Rooms
Customized modular clean room GMP sterile cleaning 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