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1. Document Information: Form ID, date, revision number, and document control information as per SASO requirements
2. Evaluator Information: Details of the person conducting the quality assessment, including name, position, department, and qualifications
3. Subject of Evaluation: Identification of the product, process, or service being evaluated, including relevant codes and specifications
4. Evaluation Criteria: Detailed listing of quality parameters to be assessed, with clear measurement scales and acceptance criteria
5. Compliance Assessment: Checklist or rating system for each quality criterion, including pass/fail or numerical scoring options
6. Observations and Findings: Space for detailed notes on specific observations, non-conformities, or exceptional performance
7. Corrective Actions: Documentation of required improvements, timeline for implementation, and follow-up procedures
8. Final Assessment: Overall evaluation result, including summary scores and final determination
9. Authorization: Signatures section for evaluator, reviewer, and other required authorities
1. Previous Evaluation Reference: Include when this is a follow-up evaluation to reference previous findings and track improvements
2. Risk Assessment: Add when evaluating high-risk products or processes requiring specific safety considerations
3. Customer Requirements: Include when evaluation involves specific customer specifications or requirements
4. Environmental Compliance: Add when evaluating processes with environmental impact considerations
5. Islamic Compliance Declaration: Include when evaluating products or processes that need to meet Halal or Islamic requirements
6. Statistical Analysis: Add when quantitative analysis of quality metrics is required
1. Evaluation Criteria Matrix: Detailed breakdown of evaluation criteria, including measurement methods and acceptable ranges
2. Reference Standards: List of applicable Saudi and GCC standards, specifications, and regulatory requirements
3. Documentation Checklist: List of required supporting documents and records to be reviewed during evaluation
4. Non-Conformance Report Template: Standard format for documenting and categorizing quality issues
5. Corrective Action Plan Template: Structured format for documenting remedial actions and timelines
6. Photo Documentation: Template for including visual evidence of findings where applicable
Manufacturing
Food and Beverage
Pharmaceuticals
Construction
Automotive
Electronics
Healthcare
Chemical Processing
Textiles
Consumer Goods
Oil and Gas
Mining
Aerospace
Quality Assurance
Quality Control
Production
Operations
Compliance
Manufacturing
Research and Development
Laboratory
Regulatory Affairs
Engineering
Health and Safety
Process Control
Quality Assurance Manager
Quality Control Inspector
Production Supervisor
Operations Manager
Compliance Officer
Quality Systems Auditor
Process Engineer
Manufacturing Manager
Technical Director
Quality Analyst
HSE Manager
Laboratory Manager
Regulatory Affairs Specialist
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