Constant temperature and humidity test chamber is a kind of test to investigate whether there is migration or adsorption between the drug package and the drug, and then affect the quality of the drug.The equipment fully meets the requirements of the new GMPspecification and is widely used in bioengineering, pharmaceutical enterprises, scientific research institutions, colleges and universities, laboratories of production enterprises, etc.

Constant temperature and humidity test chamber (Type A) is a kind of test to investigate whether there is migration or adsorption between the drug package and the drug, and then affect the quality of the drug. The equipment fully meets the requirements of the new GMP specification and is widely used in bioengineering, pharmaceutical enterprises, scientific research institutions, colleges and universities, laboratories of production enterprises, etc.

High and low temperature test chamber is to examine whether the migration or adsorption phenomenon occurs between the pharmaceutical package material and the drug, which in turn affects the quality of the drug and a test; The equipment is in full compliance with the new version of the GMP specification requirements, widely used in biological engineering, pharmaceutical enterprises, scientific research institutions, universities and colleges, production enterprises laboratory; Translated with DeepL.com (free version)

A walk-in constant temperature and humidity chamber is a large-scale environmental testing equipment that controls temperature and humidity through manual means, simulates various environmental conditions, and tests the adaptability and stability of the product Application: Widely used in electronic product manufacturing, automotive, chemical, aerospace, environmental testing and other industries. Meets the requirements of GB/T10586-2006 and JJF1101-2019 standards

Stability test chamber is to investigate the law of drug changing with time under the influence of temperature and humidity. It provides scientific basis for the conditions of production, packaging, storage and transportation of drugs. The equipment fully meets the requirements of the new GMP specification and is widely used in bioengineering, pharmaceutical enterprises, scientific research institutions, colleges and universities, laboratories of production enterprises, etc.Drug stability test chamber

Stability test chamber(Type A) is to investigate the law of drug changing with time under the influence of temperature and humidity. It provides scientific basis for the conditions of production, packaging, storage and transportation of drugs. The equipment fully meets the requirements of the new GMP and FDA specifications, and is widely used in bioengineering, pharmaceutical enterprises, scientific research institutions, colleges and universities, production enterprise laboratories, etc.

The comprehensive drug stability test chamber is to investigate the time-varying regularity of drugs under the influence of temperature, humidity and light, and to provide scientific basis for the production, packaging, storage and transportation conditions of drugs.

The Comprehensive stability test chamber (Type A) is to investigate the time-varying regularity of drugs under the influence of temperature, humidity and light, and to provide scientific basis for the production, packaging, storage and transportation conditions of drugs.

Strong light drug stability test chamber is to investigate the law of the drug changing with time under the influence of temperature and light. It provides a scientific basis for the production, packaging, storage and transportation conditions of drugs.

The high light stability test chamber (Type A)is mainly used to investigate the changes of drugs over time under the influence of temperature and light, providing scientific basis for the production, packaging, storage, and transportation conditions of drugs. At the same time, the expiration date of drugs is established through experiments, which is suitable for testing the influencing factors of drugs.

The comprehensive bright light stability test chamber is mainly used to examine the changes of drugs over time under the influence of temperature, humidity, and light, providing scientific basis for the production, packaging, storage, and transportation conditions of drugs. At the same time, the validity period of drugs is established through experiments, which is suitable for testing the influencing factors of drugs, accelerated testing, and long-term testing;

Comprehensive bright light stability test chamberr (Type A) or drugs (Type A) is mainly used to investigate the changes of drugs over time under the influence of temperature, humidity, and light, providing scientific basis for the production, packaging, storage, and transportation conditions of drugs. At the same time, the expiration date of drugs is established through experiments, which is suitable for testing the influencing factors, accelerated testing, and long-term testing of drugs;