SeverityPreventiveMaintenanceCertificate ofConformance(CoC)NonconformanceRiskAssessmentQualityPolicyCorrectiveandPreventiveAction(CAPA)OpportunityForImprovement(OFI)ExternalAuditDeviceMasterRecord(DMR)RootCauseCalibrationInternationalOrganizationforStandardization(ISO)SupplierIncomingInspectionCriteria(IIC)InternalAuditGoodDocumentationPractice (GDP)ChangeOrder(CO)ComplaintObservationMaterialReviewBoard(MRB)ContinuousImprovementCritical toQuality(CTQ)QuarantineQualityManagementSystem(QMS)DesignTransferFood andDrugAdministration(FDA)NonconformingMaterialTrainingFileReworkSeverityPreventiveMaintenanceCertificate ofConformance(CoC)NonconformanceRiskAssessmentQualityPolicyCorrectiveandPreventiveAction(CAPA)OpportunityForImprovement(OFI)ExternalAuditDeviceMasterRecord(DMR)RootCauseCalibrationInternationalOrganizationforStandardization(ISO)SupplierIncomingInspectionCriteria(IIC)InternalAuditGoodDocumentationPractice (GDP)ChangeOrder(CO)ComplaintObservationMaterialReviewBoard(MRB)ContinuousImprovementCritical toQuality(CTQ)QuarantineQualityManagementSystem(QMS)DesignTransferFood andDrugAdministration(FDA)NonconformingMaterialTrainingFileRework

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