Climatic test chamber for drug stability test

When testing the stability of drugs according to the ICH (International Coordination Conference) guidelines, the drugs must be placed under the specified climatic conditions.

600, 1300 and 2000 are special test boxes for the laboratory. They are also a supplement to the spacious walk-in test box.

characteristic

The internal fittings are all made of stainless steel, so it can provide storage areas of 2.07m2 (VP 600), 4.14m2 (1300) and 6.21m2 (2000) when the standard 6, 12 or 18 loose shelves are used.

The working range of the test chamber fully meets the requirements of ICH code Q1A.

This series of test chamber also allows users to test within the performance range of other systems according to the specification requirements.

The temperature and humidity can be controlled by using high-precision sensors and specially designed control devices.

The control system can respond quickly to correct the set value changes caused by the following factors

Influence of contents of the test chamber (water vapor absorbed or released by the sample or its packaging)

External influences (e.g. laboratory temperature, door opening)

application

The international coordination meeting (ICH) is composed of the pharmaceutical industry representative committee, scientists and authoritative institutions. It specifies the function, performance and record requirements of stability tests conducted in the pharmaceutical industry in the ICH guidelines. Europe, Japan and the United States have reached a consensus on the general stability test.

The purpose of such tests is to collect information to provide recommendations on the stability of the substance or drug product. The ultimate goal is to verify the chemical, microbiological and physical properties of the sample after exposure to a given temperature and humidity for a certain period of time.

Scientific research institutions and laboratories

Drugs and cosmetics