Corrective Action in Manufacturing | ISO 9001 & AS9100 CAPA Explained
Learn how to manage Corrective Actions in Manufacturing using the SimpleManufacturing ERP Software.
This step-by-step tutorial shows you how to create a corrective action, assign root cause analysis, track action plans, and verify effectiveness.
Corrective actions are essential for compliance with ISO 9001 and AS9100 standards, supporting CAPA (Corrective and Preventive Action) processes, and driving continuous improvement in manufacturing.
📌 What you’ll learn in this video:
✅ When to create a corrective action
✅ Key elements of corrective actions
✅ Containment vs. Corrections explained
✅ Root cause analysis in ERP
✅ Tracking action plans and verifying effectiveness
✅ Ensuring compliance with ISO 9001 & AS9100
Perfect for quality managers, auditors, and manufacturing teams focused on corrective and preventive action (CAPA).
🔗 Learn more about SimpleManufacturing ERP: https://www.simplemanufacturing.com
🔗 Explore corrective action best practices: https://www.simplemanufacturing.com/c...
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⏱️ Video Chapters:
00:00 Intro - Corrective Action in Manufacturing
00:35 What is a Corrective Action?
01:15 Containment vs Corrections
02:05 Creating a Corrective Action in ERP
03:30 Assigning Root Cause Analysis
04:40 Tracking Action Plans
05:45 Verifying Effectiveness
06:30 Compliance with ISO 9001 & AS9100
07:15 Wrap-Up & Next Steps
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