Medicine Stability Test Chamber

1.Application

The drug stability test chamber is suitable for the stability inspection and testing of pharmaceutical enterprises' drugs and new drugs, meeting the technical conditions specified in the principles of GMP, FDA, and ICH for long-term testing, intermediate conditions, accelerated testing, and high and low temperature humid heat testing.

2.Features

Temperature range: 0.0 ℃~65.0 ℃

Humidity range: 20.0% RH~95.0% RH

Controller: Adopting a touch screen temperature and humidity control instrument, it integrates functions such as printing, exporting data from a U等 flash drive, communication, cumulative running time, and alarm prompts.

Authorization and audit trail: With three-level password authorization, audit trail, and electronic signature functions.

Data storage: Electronic data can be stored for about 5 years.

Heating system: Electric heater.

Humidification system: electric steam humidifier.

Data storage: it can record historical temperature and humidity spreadsheet data and historical curve.

Printer: Micro needle printer, which can print temperature and humidity data in real-time. The printing methods are divided into table and curve printing methods, and can print device number, Beijing time, and printing interval time (adjustable).

Refrigeration method: Two sets of thermal refrigeration compressor units, controlled in two groups, environmentally friendly refrigerant R134a.

Safety protection: Independent overtemperature protection function.

Inner chamber material: Mirror stainless steel material.

Test hole: with silicone plug φ 50mm lead test hole.

Alarm system: WeChat, SMS, and phone alarms are used.

Box door: The inner door is made of tempered glass, and the outer door is an integral door.

3.Parameters (HZK-SD-S series)