deviation investigation – Pharma GMP

Root Cause Analysis for GMP Non-Conformities

digi — Wed, 03 Sep 2025 06:00:35 +0000

Root Cause Analysis for GMP Non-Conformities Effective Root Cause Analysis for GMP Non-Conformities Introduction: Why This Topic Matters for GMP Compliance Non-conformities in Good Manufacturing Practice (GMP) are inevitable in complex pharmaceutical manufacturing environments. Deviations, failures, and unexpected outcomes occur despite best efforts. Regulatory bodies such as the FDA, EMA, and WHO expect that when...

Never Skip Root Cause Analysis During GMP Deviation Investigations

digi — Tue, 27 May 2025 05:09:43 +0000

Never Skip Root Cause Analysis During GMP Deviation Investigations Root Cause Analysis Is Mandatory in All GMP Deviation Investigations Remember: Every deviation must undergo root cause analysis to implement meaningful corrective and preventive actions (CAPAs). Why This Matters in GMP When deviations occur, simply documenting them is not sufficient—underlying causes must be identified and addressed...

Review Equipment Logbooks for Completeness During GMP Audits

digi — Thu, 15 May 2025 00:46:18 +0000

Review Equipment Logbooks for Completeness During GMP Audits Ensure Equipment Logbooks Are Complete Before Every Audit Remember: Incomplete or inconsistent logbooks can jeopardize audit outcomes—always verify records are complete and current. Why This Matters in GMP Equipment logbooks document the history of usage, cleaning, calibration, and maintenance for every critical asset in a GMP facility....