What is the maximum allowed humidity in the room for sterile compounding?

For sterile compounding, maintaining appropriate humidity levels is crucial to prevent contamination and maintain the integrity of the compounding environment. The maximum allowed humidity level in the room is set at 60% or lower. This limit is established to minimize the risk of microbial growth and maintain appropriate conditions for the storage of sterile materials and products.

Humidity levels that exceed this threshold can create a favorable environment for the growth of mold, bacteria, and other contaminants that could compromise the sterility of compounded preparations. Furthermore, excessive moisture can affect the stability of certain pharmaceuticals, potentially leading to degradation or changes in their efficacy.

Ensuring that the humidity remains at or below 60% is essential for achieving compliance with the standards and guidelines set forth by regulatory bodies in sterile compounding practices. This helps guarantee a safe and effective environment for both patients and healthcare providers involved in the compounding process.