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NSF: Essential Rules When Investigating GMP Deviations During Sterile Processing

Published 12 June 2017 | By NSF Health Sciences Pharma Biotech PBR

This white paper by John Johnson outlines the key attributes to consider during sterile products manufacturing. It also details five key non-negotiables for investigating pharmaceutical GMP deviations or deficiencies in sterile processing.

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NSF: Essential Rules When Investigating GMP Deviations During Sterile Processing