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What Would Be The Temperature And Humidity For Iso 8 Clean Room?

What Would Be The Temperature And Humidity For Iso 8 Clean Room?

2023-12-01



WHAT IS ISO 8 CLEAN ROOM

A clean room is a special environment whose design and maintenance need to meet strict standards and requirements. ISO 8 is one of the classification of clean rooms, which specifies the air cleanliness and related test methods in clean rooms. The main concern of ISO 8 clean rooms is to control the number of particles in the air to ensure that the environment meets certain cleanliness requirements.

Temperature and humidity are among the important parameters in clean rooms, as they influence the number of particles in the air and microbial growth. Generally speaking, the temperature and humidity in a clean room need to be controlled within a certain range to maintain the stability and cleanliness of the environment. However, the specific temperature and humidity ranges will vary depending on different application scenarios and environmental conditions.

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TEMPERATURE AND HUMIDITY SPECIFICATIONS FOR CLEAN ROOM IN VARIOUS INDUSTRIES

In an ISO 8 clean room, the control of temperature and humidity is crucial to maintaining the cleanliness and stability of the environment. The temperature of an ISO 8 clean room needs to be controlled between 20-24 degrees Celsius, and the humidity needs to be controlled between 45-65%. Such a temperature and humidity range can effectively reduce the number of particles in the air and prevent the growth and spread of microorganisms. For various industries, the temperature and humidity have a range for different products. In biopharmaceuticals industry, the relative humidity requirement for hygroscopic drugs is 45% -50% RH (in summer), solid preparations such as tablets are 50% -55% RH, and water injections and oral liquids are 55% -65% RH. This is beneficial for better control of the production quality of drugs.

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AIR CONDITIONING AND HUMIDITY CONTROL SYSTEMS

In order to maintain such a temperature and humidity range, ISO 8 clean rooms are usually equipped with professional air conditioning systems and humidity control systems. These systems ensure the stability and cleanliness of the environment by regulating the temperature and humidity of the air. At the same time, these systems also require regular maintenance and inspection to ensure their normal operation and effectiveness.

In addition to temperature and humidity control, ISO 8 cleanrooms also require air purification. This can be achieved through the use of HEPA filters, UV disinfection and other measures. These measures can further reduce the number of particles and microorganisms in the air, ensuring the cleanliness and safety of the environment.

In short, the temperature and humidity control of ISO 8 clean rooms is one of the important factors to ensure the cleanliness and stability of the environment. In order to maintain the appropriate temperature and humidity range, professional air conditioning systems and humidity control systems need to be equipped with regular maintenance and inspections. At the same time, air purification is also required to ensure the cleanliness and safety of the environment.

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ISO 8 CLEANROOM SOLUTION BY SZ PHARMA

SZ PHARMA is a leader in the field of clean rooms and has gathered many experts with profound knowledge in this field. With our rich professional knowledge and practical experience, we can help you solve various problems encountered in the design, construction, commissioning and maintenance of clean rooms. Whether you are building a new cleanroom or need to solve a difficult problem in an existing cleanroom, we can provide you with professional guidance and advice. Our team will be dedicated to providing you with full service to ensure that your clean room project progresses smoothly and achieves expected goals. Cooperating with many industry-leading companies, we always adhere to customer-centeredness and provide you with the best quality services. Let us work together to create brilliance!



Suzhou Pharma Machinery Co.,Ltd.

2023/12/01

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