The temperature and humidity requirements of the drug warehouse?

Should be stored in the appropriate library according to the temperature and humidity requirements of the drugs, drug business enterprises of all types of drug storage should be maintained at a constant temperature. For each type of drug, according to the requirements of the storage conditions of the drug labeling, were stored in a cold storage (2-10 ℃), cool storage (below 20 ℃) or room temperature library (0-30 ℃), the relative humidity of each library should be maintained between 45% -75%.

The temperature range required by the establishment of the cold storage, cool storage and room temperature library, should be used to ensure the quality of medicines, in line with the principle of the prescribed storage conditions for medicines, scientific and reasonable settings, that is, the operation of the drugs labeled should be stored in what temperature and humidity, should be set up in the corresponding temperature and humidity range of the warehouse. Such as the operation of drugs labeled as 15-25 ℃ storage, should be set up 15-25 ℃ constant temperature warehouse.

For the identification of more than two different temperature and humidity storage conditions of the drugs, generally should be stored in a relatively low-temperature library, such as a drug labeled storage conditions: 20 ℃ below the expiration date of 3 years, 20-30 ℃ expiration date of 1 year, the drug should be stored in a cool library.

Extended information:

. p>Management specification of drugs:

Drug quality compliance is not only product quality in line with the registered quality standards, but also to make the whole process in line with the "Good Manufacturing Practice" (referred to as GMP).

"Good Manufacture Practice" (GMP) is a basic guideline for drug production and quality management, applicable to the whole process of drug preparation production and the production of APIs affect the quality of the finished product in the key processes. The vigorous implementation of pharmaceutical GMP is to maximize the avoidance of contamination and cross-contamination in the process of drug production, reduce the occurrence of various errors, is an important measure to improve the quality of drugs.

Baidu Encyclopedia- Drugs

Baidu Encyclopedia- Drug Storage