Customization: | Available |
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Temperature Control Range: | 0-65ºC |
Volume: | 150L/250/400L |
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Scope of application:
It is suitable for pharmaceutical enterprises to accelerate test and long-term test of drug failure evaluation. It is the ideal equipment for GMP certification and drug stability testing of pharmaceutical factory.
Structural features: It is suitable for pharmaceutical enterprises to evaluate drug failure, accelerate test and long-term test, which is the ideal equipment for GMP certification and drug stability test.
The right side of the box is equipped with a silicon resin material testing hole and block cap to facilitate the testing and use of the instrument: Compliance with national pharmacopoeia requirements and GB/ t10586-2006 standards, and related standards such as FDA,EN,ICN, etc. (CGMP/ICN/ 38/95/q1a and Q1B). According to the pharmacopoeia! It is necessary to test the stability of the drug in the comprehensive environment such as temperature, humidity and illumination at a certain time.
microcomputer intelligent control
1. User password control, built-in multi-function memory menu, simultaneously with multi-stage (up to 16) device connection with the standard RS485 interface, real-time monitoring; 2. Programmable multi-stage control to meet the customer's choice requirements, as many as 30 temperature and humidity, light intensity control range setting; 3. All the setting operations have the confirmation voice prompt and easy to operate; 4. Remote control with microcomputer software, and professional matching operation of ALLSENS programmable software (optional)