Why do we expose media plates in the cleanroom area for 4 hours?
Media plates are exposed in the main areas of activity and positioned to capture the maximum amount of particles.
Large particles tend to settle faster on the plates due to gravitational force. Smaller particles, however, take some time in settling due to factors such as air currents which drive them ...
Cleanroom
Clean rooms are defined as especially constructed, environmentally controlled enclosed spaces with respect to airborne particulates, temperature, humidity, air pressure, air flow patterns, air motion, vibration, noise, viable (living organisms) and lighting.
Particulate control includes:
– Particulate ...
Cleanroom Classifications
Cleanroom classifications are established by the measurement of Number of particles 0.5 micron and larger that are contained in 1 m³ of sampled air. Classification is given on two different conditions:
1. At rest:
At rest means all the equipment are installed in a clean room and HVAC system is operational ...
Clean Room
Cleanroom: As the name itself indicates, A cleanroom is a room in which the concentration of airborne Particle is controlled. Cleanroom applications are mainly in, Pharmaceutical industry, Hospitals, Biotech industry, Semiconductor industry, Microelectronic industry etc.
Clean rooms are classified according ...
Cleanroom Contamination
For decades, non-functional particle cleaning levels have been closely measured and monitored in pharmaceutical cleanrooms, in an effort to improve drug quality and save patient lives. In parallel effective microbial contamination levels have also been closely measured and monitored through the use ...
4 Common Cleanroom Contaminents
Maintaining a cleanroom environment has unique challenges because it is constantly exposed to a number of pollutants. To stabilize your company’s particle count, it’s important to identify your main sources of pollution. Although these sources may vary from one organization to another, the ...
Types of cleanroom pass boxes
When designing modern cleanrooms and laboratories, special attention needs to be paid to material flow. Whether it is ISO 14611 or a GMP application, there are very specific requirements that dictate where and how the material enters and exits the room.
This is when the pass box comes into the picture. ...

