ExternalAuditGoodDocumentationPractice (GDP)ContinuousImprovementIncomingInspectionCriteria(IIC)Certificate ofConformance(CoC)NonconformingMaterialQualityManagementSystem(QMS)InternationalOrganizationforStandardization(ISO)PreventiveMaintenanceRootCauseQuarantineComplaintCorrectiveandPreventiveAction(CAPA)DesignTransferNonconformanceOpportunityForImprovement(OFI)RiskAssessmentSeverityObservationCalibrationChangeOrder(CO)SupplierReworkFood andDrugAdministration(FDA)MaterialReviewBoard(MRB)DeviceMasterRecord(DMR)InternalAuditCritical toQuality(CTQ)QualityPolicyTrainingFileExternalAuditGoodDocumentationPractice (GDP)ContinuousImprovementIncomingInspectionCriteria(IIC)Certificate ofConformance(CoC)NonconformingMaterialQualityManagementSystem(QMS)InternationalOrganizationforStandardization(ISO)PreventiveMaintenanceRootCauseQuarantineComplaintCorrectiveandPreventiveAction(CAPA)DesignTransferNonconformanceOpportunityForImprovement(OFI)RiskAssessmentSeverityObservationCalibrationChangeOrder(CO)SupplierReworkFood andDrugAdministration(FDA)MaterialReviewBoard(MRB)DeviceMasterRecord(DMR)InternalAuditCritical toQuality(CTQ)QualityPolicyTrainingFile

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