Stability Test Chamber

Stability Test Chamber

Drug Stability Test Chamber It can be used in painstaking research of pharmaceutical industry, medical industry, biological technology industry and other industries related to life science. To prove the shelf life of a drug in a certain market, the manufacturer must store it at a relevant temperature and humidity for a specified time.
 
According to GMP principle, constant and stable test conditions of 25°C/60% RH shall be maintained. The drug stability test chambers in the stability test system field of pharmaceutical industry, the standard of 40°C/75% RH shall remain for 6 months in acceleration test, mainly simulating the temperature, humidity and illumination.
 
The most common conditions are 25°C/60% RH. For a new product accelerated conditions may be 40°C/75% RH. Other conditions include 30°C/65% RH, 30°C/35% RH and 25°C/40% RH. Another condition is 5°C ±3°C for products intended to be stored in a refrigerator. For products intended for storage in a freezer the test conditions are -20°C ±5° C.
 

Model DescVolumeSize (W*D*H/ mm)Voltage  (V/HZ)PowerTemperatureNet Weight
WE-25C09090L620*545*0845220/50,60 V87W-10 ~-25 ºC45 kgs
WE-25C135135L620*540*1120220/50,60 V100W-10 ~-25 ºC55 kgs
WE-25C208208L620*600*1775220/50,60 V115W-10 ~-25 ºC75 kgs
WE-25C270270L620*600*1750220/50,60 V120W-10 ~-25 ºC90 kgs
WE-25C530530L950*850*2000220/50,60 V150W-10 ~-25 ºC235 kgs

 

 

 

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Wewon Environmental Chambers Co., Ltd. as a manufacturer and supply humidity and temperature testing chambers for abroad partners many years ! The mainly product from Wewon Environmental Chambers Co., Ltd. : temperature humidity chambers, walk-in chambers, thermal shock chambers, xenon test chambers, ozone chambers, & vibration test systems.

 

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