CAPA in Pharmaceutical Industry | Corrective Action & Preventive Action Explained | Pharma QA GMP

In this video, I have explained Corrective Action and Preventive Action (CAPA) in a simple, practical, and GMP-compliant manner as followed in the pharmaceutical industry.


This video is extremely useful for: ✔ Pharma QA professionals
✔ GMP & Compliance teams
✔ Validation & Production teams
✔ Pharma freshers & students
✔ Anyone facing audit observations, deviations, OOS, or complaints


🔍 Topics Covered in This Video:

What is CAPA in pharmaceutical industry?
Difference between Corrective Action vs Preventive Action
Regulatory expectations as per WHO GMP & ICH guidelines
How CAPA is linked with:
Deviations
OOS
Audit observations
Complaints
Change control
How to prepare effective & sustainable CAPA
Common CAPA mistakes observed during audits


🎯 Who Should Watch This Video?

Pharma QA & QC professionals
GMP trainees & auditors
Pharma freshers preparing for interviews
Professionals working in regulated environments

📌 This video helps you understand CAPA not only for documentation but also for real GMP implementation.


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🔗    • CAPA in Pharmaceutical Industry | Correcti...  


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📚 All Pharma QA, Validation & GMP learning at one place.

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