QualityManagementSystem(QMS)CorrectiveandPreventiveAction(CAPA)QuarantineInternalAuditOpportunityForImprovement(OFI)NonconformanceQualityPolicyReworkRiskAssessmentCritical toQuality(CTQ)InternationalOrganizationforStandardization(ISO)ObservationSeverityDesignTransferChangeOrder(CO)GoodDocumentationPractice (GDP)IncomingInspectionCriteria(IIC)DeviceMasterRecord(DMR)SupplierNonconformingMaterialContinuousImprovementCertificate ofConformance(CoC)RootCauseFood andDrugAdministration(FDA)CalibrationComplaintMaterialReviewBoard(MRB)PreventiveMaintenanceTrainingFileExternalAuditQualityManagementSystem(QMS)CorrectiveandPreventiveAction(CAPA)QuarantineInternalAuditOpportunityForImprovement(OFI)NonconformanceQualityPolicyReworkRiskAssessmentCritical toQuality(CTQ)InternationalOrganizationforStandardization(ISO)ObservationSeverityDesignTransferChangeOrder(CO)GoodDocumentationPractice (GDP)IncomingInspectionCriteria(IIC)DeviceMasterRecord(DMR)SupplierNonconformingMaterialContinuousImprovementCertificate ofConformance(CoC)RootCauseFood andDrugAdministration(FDA)CalibrationComplaintMaterialReviewBoard(MRB)PreventiveMaintenanceTrainingFileExternalAudit

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