Compressed air systems are a critical component of many pharmaceutical manufacturing facilities. With any new system creation, addition, or change, a validation should be performed to ensure the ...

This article outlines guidelines for the testing of high pressure gases utilized in cleanrooms according to the cleanliness limits stated in the FDA cGMP guidelines, the ISO 14644-1 cleanroom ...

New and in-service fluids encounter solid contamination from machinery burrs, filter deterioration and blow-by, worn mechanical seals, dirt and sand from the environment, and solid oxides from ...

An important part of any machine conditioning program is particle counting. There are a number of existing tools to monitor and track the quantity and severity of the contamination, whether it is a ...