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 ...
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 ...
Beckman Coulter Life Sciences announced today that the MET ONE 3400+ portable air particle counter is now available to help GMP cleanroom users simplify their routine environmental monitoring and ...
Pharma cleanrooms are those rooms that need to meet the code of good manufacturing practices (GMP) requirements as defined in the sterile code of GMP towards compliance, according to experts. A pharma ...
WILMINGTON, Mass.--(BUSINESS WIRE)--DTG, the leading provider of industrial-strength power systems and mobile workstation solutions, today launched the Cleanroom PowerStation. The mobilized, ...
Chrysalis lists among its partners early-stage biotechnology companies, contract research organizations, top-10 pharmaceutical firms, and various other life sciences stakeholders. Chrysalis, a good ...
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