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.
A practical, end-to-end toolkit for solving quality problems in regulated environments. Build a quality culture, turn problems into focused projects, generate and prioritise ideas, listen to patients and customers, map the real process, check that your data can be trusted, and make it speak with Pareto charts, trends, control charts and capability studies. Then dig to the root cause, test what really drives results, prevent problems with FMEA, and hold the gains with control plans.
Run investigations that inspectors trust: how deviations flow into the CAPA system, detection, impact assessment and triage, problem definition, root cause tools, human error and laboratory OOS investigations, CAPA plans with effectiveness checks, and clear investigation reports.
Build a CAPA system that actually prevents recurrence: maturity assessment, problem statements, root cause analysis, action planning, effectiveness checks, KPIs, governance and continual improvement.
نظام الإجراءات التصحيحية والوقائية — دورة فيديو تفاعلية بتعليق صوتي إنجليزي ونصوص ثنائية اللغة (إنجليزي / عربي).
Course modules
- What CAPA Really Is
- Measuring CAPA Maturity
- Documentation and Problem Identification
- Root Cause Analysis
- Corrective and Preventive Actions
- Effectiveness Checks and Metrics
- Governance and Leadership
- Improving Your CAPA System
Instructor: Rafat Alghubari — GxPeria Founder & MD.
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