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 ...
Cleanrooms are built to consider air flow, air pressure, temperature, and other important points, but sometimes errors occur and maintaining a noncontaminated environment can be a challenge when ...
Routine Environmental Monitoring in GMP cleanrooms is a manual process and is usually complex, involving thousands of sample data points per month, manual data transcription and all too frequently ...
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