A new generation of drug stability test equipment, set design and production company for many years of experience, the introduction of German technology digestion. Unable to break through the existing domestic drug chamber long continuous operation defects are pharmaceutical 高标准 certification of the necessary equipment. Uses: In the scientific method to create an evaluation of drug failures take a long time stable temperature, humidity and light environment for pharmaceutical companies for medicines and accelerated testing of new drugs, long-term test, humidity test and glare testing, Pharmaceutical companies are the best choice for drug stability testing program. Features: ◆ Humanized design ● new CFC-free design, high efficiency, low energy consumption, promote energy conservation, so that you are always at the forefront of a healthy life. ● microcomputer control, stability control, accurate and reliable, the use of 304 stainless steel, semi-circular curved corners, easy to clean, easy to operate. ● Unique air circulation, ensuring internal wind distribution studio. The left side of the box there is a test hole diameter of 25mm. ◆ ● ensure continuous operation of two imported compressor automatically switches to ensure continuous operation for a long time drug test failure does not occur. Unable to break the domestic pharmaceutical chamber long continuous operation defects. ● continuous operation without defrosting, avoiding the use of the process, because of fluctuations in temperature and humidity inside the cream produced. ◆ Quality Assurance ● temperature and humidity control, compressor, circulating fans and other key components are imported products, with a long-running stable, safe, and reliable. ◆ security features ● Independent limit temperature alarm system that can sound and light alarm prompts the operator to ensure the safe operation of the laboratory is not an accident. ● low or high temperature and over-temperature alarm, high humidity and low alarm. ◆ imported humidity sensor humidity sensor ● selection can run at a high temperature, to avoid frequent replacement of wet and dry bulb wet with annoyance. ◆ UV sterilization system (optional) ● UV germicidal lamp placed inside the wall, inside the box can be disinfected on a regular basis, can effectively kill the pan cabinets circulating air and water vapor floating bacteria, thereby effectively preventing drug contamination during the test. ◆ illumination automatic monitoring and control (optional) ● beyond the current domestic stability chamber illumination defects can not be monitored and controlled using a light sensor for monitoring does not adjustable, reduce the lamp illumination attenuation caused by aging and experimental error. ◆ data recording and fault diagnosis display ● When the chamber fails, an error message will display dynamic, chamber operational failure at a glance. ● You can connect a printer or 485 communication interface, temperature and time curves recorded with a computer and printer for test data storage and playback process provide a strong guarantee. Programmable touch screen controller (optional) ● with large touch-screen display screen, the screen is simple to operate, easy to edit programs. ● The controller interface to choose from in English, instant graphs can be displayed operation. ● has 100 sets of program segment capacity 999 1000 cycle steps, each time setting a maximum of 99 hours and 59 minutes. ● After the input data and test conditions, the controller has a screen lock feature to avoid human touch and downtime. ● With PID automatic calculation function, you can change the temperature and humidity conditions are corrected immediately, so that more precise and stable temperature and humidity control. ● with RS-232 or RS-485 communication interface, the computer design program, monitor the testing process and execute switch functions. Execute and meet the standard: Pharmacopoeia 2010 edition of drug stability testing guidelines and GB / T10586-2006 the terms of manufacturing ★ stability test conditions: ICH guidelines, the functionality, performance and documentation, 高标准 and FDA requirements are defined. Europe, Japan and the United States agreed to develop a common stability tests, the goal of these tests is a collection of information, as to develop a recommendation on the stability of raw materials or drugs, the ultimate goal is for the specified period, to prove the drug is exposed to temperature, humidity, light or integrated environment effectiveness. ★ stay kind of long-term storage conditions of stability testing: Temperature: + 25 ℃ ± 2 ℃ Humidity: 60 ± 5% RH Duration: 12 months accelerated stability test ★ storage conditions Temperature: + 40 ℃ ± 2 ℃ Humidity: 75 ± 5% RH Duration: 6 months glare illumination conditions: 4500 ± 500LX