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Pharmaceutical Industry

Source:普爱德环保科技Time:2016-7-28 15:26:20

Pharmaceutical production quality management standards Article XVII: clean (area) temperature and relative humidity should be compatible with the pharmaceutical production process requirements. No special requirements, the temperature should be controlled at 18 ~ 26 ℃, relative humidity control at 45 ~ 65%. To meet this requirement, the pharmaceutical factory production workshop must be set up air conditioning and purification devices, temperature and humidity control through the appropriate heating, cooling and add / dehumidification device to achieve. In order to meet the GMP requirements.

Drugs should be stored in accordance with the provisions of the special library, classified storage. Store in accordance with the temperature and humidity requirements of drugs stored in the corresponding library.

Pharmaceutical production enterprises review and evaluation criteria: 25.7 production environment no air purification requirements of the in vitro diagnostic reagent products, whether the production workshop temperature and humidity control.

Production implementation of a rule: there is a requirement for air drying operation room should be equipped with air-drying equipment to ensure that the material will not be damp deterioration, regular dehumidification equipment maintenance, monitoring indoor air humidity.

Thus, the temperature and humidity of the pharmaceutical industry requires strict control, and runner dehumidifier is an ideal equipment to control humidity.


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