DeviceMasterRecord(DMR)RiskAssessmentCertificate ofConformance(CoC)CalibrationInternalAuditRootCauseChangeOrder(CO)OpportunityForImprovement(OFI)ComplaintInternationalOrganizationforStandardization(ISO)NonconformingMaterialNonconformanceQuarantineCorrectiveandPreventiveAction(CAPA)IncomingInspectionCriteria(IIC)ExternalAuditCritical toQuality(CTQ)TrainingFileFood andDrugAdministration(FDA)DesignTransferObservationSeverityQualityPolicyMaterialReviewBoard(MRB)ContinuousImprovementQualityManagementSystem(QMS)ReworkPreventiveMaintenanceSupplierGoodDocumentationPractice (GDP)DeviceMasterRecord(DMR)RiskAssessmentCertificate ofConformance(CoC)CalibrationInternalAuditRootCauseChangeOrder(CO)OpportunityForImprovement(OFI)ComplaintInternationalOrganizationforStandardization(ISO)NonconformingMaterialNonconformanceQuarantineCorrectiveandPreventiveAction(CAPA)IncomingInspectionCriteria(IIC)ExternalAuditCritical toQuality(CTQ)TrainingFileFood andDrugAdministration(FDA)DesignTransferObservationSeverityQualityPolicyMaterialReviewBoard(MRB)ContinuousImprovementQualityManagementSystem(QMS)ReworkPreventiveMaintenanceSupplierGoodDocumentationPractice (GDP)

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