ReworkDeviceMasterRecord(DMR)ComplaintRiskAssessmentContinuousImprovementExternalAuditInternationalOrganizationforStandardization(ISO)QualityPolicyIncomingInspectionCriteria(IIC)OpportunityForImprovement(OFI)NonconformanceGoodDocumentationPractice (GDP)MaterialReviewBoard(MRB)QualityManagementSystem(QMS)RootCauseObservationCalibrationPreventiveMaintenanceSupplierQuarantineFood andDrugAdministration(FDA)SeverityCritical toQuality(CTQ)TrainingFileChangeOrder(CO)InternalAuditCorrectiveandPreventiveAction(CAPA)Certificate ofConformance(CoC)NonconformingMaterialDesignTransferReworkDeviceMasterRecord(DMR)ComplaintRiskAssessmentContinuousImprovementExternalAuditInternationalOrganizationforStandardization(ISO)QualityPolicyIncomingInspectionCriteria(IIC)OpportunityForImprovement(OFI)NonconformanceGoodDocumentationPractice (GDP)MaterialReviewBoard(MRB)QualityManagementSystem(QMS)RootCauseObservationCalibrationPreventiveMaintenanceSupplierQuarantineFood andDrugAdministration(FDA)SeverityCritical toQuality(CTQ)TrainingFileChangeOrder(CO)InternalAuditCorrectiveandPreventiveAction(CAPA)Certificate ofConformance(CoC)NonconformingMaterialDesignTransfer

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