Clean Room Humidity Control

Clean Room Humidity Control

According to the standards used in the pharmaceutical industry and the institutions that define these standards, all relevant parameters such as airborne particle concentration, microbiological contamination, temperature-humidity, and pressure must be kept under control for all clean rooms subject to production. In laminar flow cabinets, the risk of contamination requires frequent monitoring of air quality. R&D laboratories working on new products and formulations determine the ideal atmospheric conditions for products.

The use of industrial dehumidifiers to achieve the required humidity conditions in facilities and strict control of indoor climate conditions means preventing quality fluctuations that may occur in products. Industrial dehumidifier integrations in clean rooms and laminar flow cabinets aim to provide the required humidity conditions regardless of ambient conditions. This eliminates the risk of moisture absorption by hygroscopically active substances used in processes. The precision of sensitive experiments conducted under correct atmospheric conditions in R&D laboratories is a factor that increases the predictability of large-scale production performance.

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