Whitepaper: GMP Cleanroom Environmental Monitoring
Posted: 15 July 2020 | Beckman Coulter | No comments yet
This whitepaper from Beckman Coulter explores GMP cleanroom routine environmental monitoring and data integrity.
Routine Environmental Monitoring in GMP cleanrooms is a manual process and can be complex, involving thousands of sample data points per month, manual data transcription and all too frequently data gaps and integrity challenges. This paper shows how the new MET ONE 3400+ non-viable air particle counter from Beckman Coulter Life Sciences can be automated to help manage these challenges.
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Biopharmaceuticals, Data integrity, Drug Delivery Systems, Environmental Monitoring, Good Manufacturing Practice (GMP), Manufacturing, QA/QC, Regulation & Legislation