🇦🇪UAE
فقدان القدرة بسبب CAPA
1 verified sources
Definition
Unresolved CAPAs block production lines, causing idle equipment and missed delivery deadlines.
Key Findings
- Financial Impact: 10% capacity loss (AED 1,000,000+ annually for mid-size firm)
- Frequency: Per unresolved high-risk CAPA
- Root Cause: Bottlenecks in manual CAPA workflows
Why This Matters
This pain point represents a significant opportunity for B2B solutions targeting Medical Equipment Manufacturing.
Affected Stakeholders
Production Managers, Engineers
Deep Analysis (Premium)
Financial Impact
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Current Workarounds
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Methodology & Sources
Data collected via OSINT from regulatory filings, industry audits, and verified case studies.
Related Business Risks
تكاليف الجودة الرديئة
AED 500,000+ annually in rework and warranty costs (industry standard 2-5% of production costs for poor quality)
غرامات عدم الامتثال لـ CAPA
AED 50,000 - 200,000 per audit failure (based on typical ISO certification penalties and lost business)
تجاوز تكاليف إدارة CAPA
40 hours/month per quality team (AED 500/hour equivalent in overtime/waste)
تجاوز التكاليف
40-80 hours/month overtime at AED 200/hr; AED 20,000+ Nafis non-compliance fees.
فقدان السعة الإنتاجية
2-5% capacity loss; AED 100,000/month idle equipment.
غرامات عدم تسجيل الأجهزة الطبية
AED 20,000-50,000 per deferred registration (consultant fees, 40-80 hours rework); 6-12 months sales delay at AED 100,000+ opportunity cost.
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