Products Description
The pharmaceutical stability test chamber, also known as the environmental test chamber, is like a miniature drug time tunnel, which can accurately simulate the various environmental conditions that drugs may encounter in the entire life cycle. From the extreme heat of the tropics to the freezing cold of the polar regions, from the dry desert to the humid and sultry rainforest climate, it can reproduce these complex and changeable environmental scenes through precise temperature and humidity control and advanced light simulation technology. Whether you need to test the chemical stability of a drug in a high temperature and humidity environment or evaluate its physical changes under light radiation, the pharmaceutical stability test chamber can meet the requirements with the exact accuracy, providing pharmaceutical companies with extremely reliable drug stability data.
Stage test
Initial stage
In the early stages of drug development, pharmaceutical stability test chambers play an indispensable and critical role. It helps researchers quickly identify drug formulations with good stability potential. The long-term simulation test of drug candidates under different environmental conditions can predict the degradation and deterioration of drugs in the storage process in advance, which provides a valuable experimental basis for optimizing drug formulation. This not only greatly shortens the cycle of drug research and development, reduces the cost of research and development, but also lays a solid foundation for clinical trials and commercial production of subsequent drugs.
Interim test
Entering the drug production process, the pharmaceutical stability test chambers has become the core weapon of quality control. Each batch of drugs must undergo a rigorous stability test before leaving the factory to ensure that it can always maintain the quality and efficacy of the standard within the specified period of validity. The pharmaceutical stability test chamber can perform accelerated stability testing and long-term stability testing of drugs in accordance with relevant international and domestic standards. In the accelerated stability test, by setting parameters such as temperature and humidity higher than the actual storage conditions, the quality change trend of drugs in the long-term storage process can be simulated in a short time, so as to quickly evaluate the stability of drugs. The long-term stability test is close to the actual storage environment, the drug for months or even years of continuous monitoring, to provide the most real and reliable data support for the validity of the drug.
Finally
For pharmaceutical companies, having a high-quality pharmaceutical stability test chambers means having a strong guarantee of market competitiveness. In the increasingly strict drug regulatory environment, only by ensuring the stable and reliable quality of drugs can we win the trust of patients and the recognition of doctors, and then in an invincible position in the fierce market competition. The pharmaceutical stability test chamber can not only help enterprises ensure the quality of their products, but also provide strong evidence support when responding to the inspection and audit of the drug regulatory department, so that enterprises can move forward more steadily on the road of compliance operation.
advantage
The pharmaceutical stability test chamber, with its excellent quality of precision, reliability and multi-function, has become an indispensable key equipment in the pharmaceutical industry. It is a loyal defender of drug quality, a powerful driving force to promote the innovation and development of pharmaceutical technology, and a solid defense line to ensure the safety and effectiveness of human drugs. Choosing a pharmaceutical stability test chamber is to choose to be responsible for drug quality and contribute to the cause of human health. Let us work together to make use of the power of this advanced equipment to create more brilliant achievements in the pharmaceutical field and write a more magnificent chapter for human health and well-being.
Product parameter
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Model |
BT-280 |
BT-2150 |
BT-2225 |
BT-2408 |
BT-2800 |
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Inner Size W×H×D(cm) |
40×50×40 |
50×60×50 |
50×75×60 |
60×85×80 |
100×100×80 |
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Outside Size W×H×D(cm) |
93×155×95 |
100×148×106 |
117×166×91 |
140×176×101 |
170×186×111 |
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Volume (V) |
80 L |
150L |
225L |
408L |
800L |
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Temp and Hum Range |
A:-20°C~150°C B: -40°C~150°C C: -60°C~150°C D: -70°C~150°C RH20%-98% |
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Function |
Fluctuation |
±0.5°C ±2.5%RH |
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Deviation |
±0.5°C-±2°C ±3%RH(>75%RH); ±5%RH(≤75%RH) |
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Controller Analytical Accuracy |
±0.3°C ±2.5%RH |
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Wind Cycling Way |
Centrifugal fan-broadband type forced air circulation |
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Refrigeration Way |
Single stage compression refrigeration |
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Refrigerator |
French Tecumseh |
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Refrigerants |
R4O4A USA DuPont environmental protection refrigerant(R23+R404) |
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Condensing Way |
Air-cooled or water-cooled |
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Water Supplying Way |
Automatic cycling water supply |
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Safety device |
Non- fuse-switch(compressor overload, refrigerant high low voltage, over-humidity and temperature protection, Protection switch,fuse stoppage warning system |
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