QualityPolicyCalibrationChangeOrder(CO)NonconformingMaterialPreventiveMaintenanceCertificate ofConformance(CoC)InternationalOrganizationforStandardization(ISO)TrainingFileContinuousImprovementGoodDocumentationPractice (GDP)OpportunityForImprovement(OFI)ComplaintQualityManagementSystem(QMS)NonconformanceMaterialReviewBoard(MRB)DeviceMasterRecord(DMR)RootCauseCorrectiveandPreventiveAction(CAPA)ReworkInternalAuditObservationExternalAuditIncomingInspectionCriteria(IIC)Food andDrugAdministration(FDA)SupplierQuarantineDesignTransferRiskAssessmentCritical toQuality(CTQ)SeverityQualityPolicyCalibrationChangeOrder(CO)NonconformingMaterialPreventiveMaintenanceCertificate ofConformance(CoC)InternationalOrganizationforStandardization(ISO)TrainingFileContinuousImprovementGoodDocumentationPractice (GDP)OpportunityForImprovement(OFI)ComplaintQualityManagementSystem(QMS)NonconformanceMaterialReviewBoard(MRB)DeviceMasterRecord(DMR)RootCauseCorrectiveandPreventiveAction(CAPA)ReworkInternalAuditObservationExternalAuditIncomingInspectionCriteria(IIC)Food andDrugAdministration(FDA)SupplierQuarantineDesignTransferRiskAssessmentCritical toQuality(CTQ)Severity

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