RootCauseSupplierCertificate ofConformance(CoC)InternationalOrganizationforStandardization(ISO)DesignTransferMaterialReviewBoard(MRB)CalibrationQuarantineQualityPolicyOpportunityForImprovement(OFI)ContinuousImprovementComplaintObservationDeviceMasterRecord(DMR)InternalAuditReworkNonconformingMaterialNonconformanceRiskAssessmentCritical toQuality(CTQ)ChangeOrder(CO)GoodDocumentationPractice (GDP)SeverityPreventiveMaintenanceFood andDrugAdministration(FDA)CorrectiveandPreventiveAction(CAPA)IncomingInspectionCriteria(IIC)ExternalAuditTrainingFileQualityManagementSystem(QMS)RootCauseSupplierCertificate ofConformance(CoC)InternationalOrganizationforStandardization(ISO)DesignTransferMaterialReviewBoard(MRB)CalibrationQuarantineQualityPolicyOpportunityForImprovement(OFI)ContinuousImprovementComplaintObservationDeviceMasterRecord(DMR)InternalAuditReworkNonconformingMaterialNonconformanceRiskAssessmentCritical toQuality(CTQ)ChangeOrder(CO)GoodDocumentationPractice (GDP)SeverityPreventiveMaintenanceFood andDrugAdministration(FDA)CorrectiveandPreventiveAction(CAPA)IncomingInspectionCriteria(IIC)ExternalAuditTrainingFileQualityManagementSystem(QMS)

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