In the pharmaceutical industry, cleanrooms are categorized based on the level of airborne particle concentration necessary to meet the cleanliness standards required for the specific manufacturing ...
Both the USA cGMP 1 and EU GMP 2 dictate that cleanroom classification must be carried out according to ISO 14644-1. The version of this ISO standard released in 1999 4 was rewritten by a group of ...
Press Trust of India on MSN
TÜV Rheinland reinforces global contamination control with clean room validation services
Comprehensive Testing, Independent Verification and International Compliance Support for High-Precision and Regulated ...
Particle measurements in ultra-pure water (UPW) systems can take a long time to return to a stable baseline after normal operations are interrupted by an event such as maintenance shutdowns. A ...
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