Skip to main content

AVITSENA

Deviation Management in GMP

Categories: Quality Systems
Wishlist Share

About Course

Manage deviations from first detection to effective CAPA. Learn what a deviation is, types and categories, risk-based classification, the end-to-end deviation process, how to write a clear deviation report, investigation and root cause analysis, impact assessment and batch disposition, CAPA, trending and metrics, and the deviation findings inspectors raise most often.

What Will You Learn?

  • What Is a Deviation
  • Types and Categories
  • Classification
  • The Deviation Process Map
  • Writing the Report
  • Investigation and Root Cause Analysis
  • Impact and Disposition
  • CAPA
  • Trending and Metrics
  • Inspection Findings

Course Content

Introduction

Module 1: What Is a Deviation

Module 2: Types and Categories

Module 3: Classification

Module 4: The Deviation Process Map

Module 5: Writing the Report

Module 6: Investigation and Root Cause Analysis

Module 7: Impact and Disposition

Module 8: CAPA

Module 9: Trending and Metrics

Module 10: Inspection Findings

Final Assessment

Earn a certificate

Add this certificate to your resume to demonstrate your skills & increase your chances of getting noticed.

selected template

Student Ratings & Reviews

No Review Yet
No Review Yet

Want to receive push notifications for all major on-site activities?

✕