Common Audit Findings Related to Chamber Calibration in Pharma
Stability chamber calibration is a core expectation in GMP-regulated pharmaceutical environments. Yet, despite well-defined protocols and validation requirements, calibration-related issues frequently appear in regulatory inspection reports, including USFDA 483s, WHO observations, and EMA audit summaries. This tutorial outlines the most common audit findings related to chamber calibration and offers actionable steps to prevent them. Whether…
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