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Deviation Handling and GMP Investigations
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Level |
Introductory |
Format |
On-site, practical, including essential theory |
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Duration |
Half-day |
Fee |
$543 |
Overview
Deviation Handling and GMP Investigations helps teams build the mindset and practical problem-solving capability required to manage deviations in a structured, compliant, and audit-ready manner. Through realistic scenarios and applied exercises, participants practice using the tools and critical thinking needed to investigate effectively, identify root causes, and prevent recurrence.
What participants will learn
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Understand the role and business impact of investigations in GMP environments
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Follow the investigation lifecycle from detection and containment through closure
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Apply root-cause analysis tools such as 5 Whys and Ishikawa diagrams
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Document investigations and CAPAs with stronger compliance awareness
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Practice investigation thinking through scenario-based problem solving and group discussion
Ideal audience:
Ideal for new hires, QA professionals, operators, supervisors, SMEs, maintenance teams, and QC staff who initiate, support, or review investigations.
Employer value:
For employers, this course strengthens investigation quality and helps teams resolve deviations more efficiently and defensibly.
Note: This module is integrated in the 1-day GMP Readiness Accelerator
