ObservationQualityManagementSystem(QMS)CorrectiveandPreventiveAction(CAPA)SupplierChangeOrder(CO)RiskAssessmentNonconformanceContinuousImprovementDesignTransferGoodDocumentationPractice (GDP)PreventiveMaintenanceQuarantineCritical toQuality(CTQ)RootCauseDeviceMasterRecord(DMR)OpportunityForImprovement(OFI)NonconformingMaterialCalibrationReworkInternationalOrganizationforStandardization(ISO)SeverityMaterialReviewBoard(MRB)Food andDrugAdministration(FDA)ExternalAuditQualityPolicyComplaintIncomingInspectionCriteria(IIC)TrainingFileCertificate ofConformance(CoC)InternalAuditObservationQualityManagementSystem(QMS)CorrectiveandPreventiveAction(CAPA)SupplierChangeOrder(CO)RiskAssessmentNonconformanceContinuousImprovementDesignTransferGoodDocumentationPractice (GDP)PreventiveMaintenanceQuarantineCritical toQuality(CTQ)RootCauseDeviceMasterRecord(DMR)OpportunityForImprovement(OFI)NonconformingMaterialCalibrationReworkInternationalOrganizationforStandardization(ISO)SeverityMaterialReviewBoard(MRB)Food andDrugAdministration(FDA)ExternalAuditQualityPolicyComplaintIncomingInspectionCriteria(IIC)TrainingFileCertificate ofConformance(CoC)InternalAudit

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