SupplierTrainingFileCorrectiveandPreventiveAction(CAPA)Certificate ofConformance(CoC)ChangeOrder(CO)QualityPolicyOpportunityForImprovement(OFI)ReworkIncomingInspectionCriteria(IIC)NonconformanceFood andDrugAdministration(FDA)DesignTransferInternationalOrganizationforStandardization(ISO)QuarantineCalibrationComplaintQualityManagementSystem(QMS)NonconformingMaterialPreventiveMaintenanceRootCauseInternalAuditRiskAssessmentExternalAuditDeviceMasterRecord(DMR)ContinuousImprovementMaterialReviewBoard(MRB)SeverityGoodDocumentationPractice (GDP)ObservationCritical toQuality(CTQ)SupplierTrainingFileCorrectiveandPreventiveAction(CAPA)Certificate ofConformance(CoC)ChangeOrder(CO)QualityPolicyOpportunityForImprovement(OFI)ReworkIncomingInspectionCriteria(IIC)NonconformanceFood andDrugAdministration(FDA)DesignTransferInternationalOrganizationforStandardization(ISO)QuarantineCalibrationComplaintQualityManagementSystem(QMS)NonconformingMaterialPreventiveMaintenanceRootCauseInternalAuditRiskAssessmentExternalAuditDeviceMasterRecord(DMR)ContinuousImprovementMaterialReviewBoard(MRB)SeverityGoodDocumentationPractice (GDP)ObservationCritical toQuality(CTQ)

Quality Week - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. Supplier
  2. Training File
  3. Corrective and Preventive Action (CAPA)
  4. Certificate of Conformance (CoC)
  5. Change Order (CO)
  6. Quality Policy
  7. Opportunity For Improvement (OFI)
  8. Rework
  9. Incoming Inspection Criteria (IIC)
  10. Nonconformance
  11. Food and Drug Administration (FDA)
  12. Design Transfer
  13. International Organization for Standardization (ISO)
  14. Quarantine
  15. Calibration
  16. Complaint
  17. Quality Management System (QMS)
  18. Nonconforming Material
  19. Preventive Maintenance
  20. Root Cause
  21. Internal Audit
  22. Risk Assessment
  23. External Audit
  24. Device Master Record (DMR)
  25. Continuous Improvement
  26. Material Review Board (MRB)
  27. Severity
  28. Good Documentation Practice (GDP)
  29. Observation
  30. Critical to Quality (CTQ)