Release 11 - The Standard for Quality Assurance software designed to evaluate and measure the clinical laboratory performance and provides clear, concise, 'inspector-ready' reports to meet all CLIA '88, CAP, JCAHO  and COFRAC requirements.  EP Evaluator® was designed by a board-certified clinical chemist specifically to meet the needs of the clinical laboratory and is used by more laboratories and more invitro diagnostics (IVD) companies than any other software of its kind.

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Version Comparisons

 
Regulatory Requirements
EP Evaluator Versions
 
CLIA
CAP
TJC
COFRAC
Standard
Pro
Accuracy and Linearity
Clinical Linearity, Calibration Verification
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Reportable Range
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Simple Accuracy
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CLSI EP6 Linearity        
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Trueness        
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Method Comparison
Alternate (Routine Quantitative)
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CLSI EP9 Method Comparison        
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Two Instrument Comparison  
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Multiple Instrument Comparison  
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Qualitative / Semi-Quantitative
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POC Glucose        
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Hematology Studies        
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Precision
Simple Precision
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CLSI EP5 Precision        
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Reference Interval
Establish
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Verify
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ROC Plots        
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Sensitivity
Limits of Blank (Analytical) *
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Limits of Quantitation (Functional) *      
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Lab Management
Cost Per Test        
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Incident Tracking        
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Inventory Management        
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Competency Assessment        
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Coagulation
Geometric Mean and VRI  
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PT/INR Method Comparison  
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Manual INR Check  
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Factor Sensitivity (FS)        
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Other
Performance Standards (TEa)        
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Carryover  
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CLSI EP10 - Preliminary Evaluation
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Interference (CLSI EP7) *
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Six Sigma Metrics        
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Average of Normals (Checks Bias)        
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Stability        
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Histogram and Descriptive Stats        
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Additional Features
Composite Reporting        
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Data Extraction from Middleware          
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Project Manageement        
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Audit Trail and Network Security          
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Implements Eight CLSI Protocols

  • EP5-A, Evaluation of Precision Performance of Clinical Chemistry Devices; Approved Guideline
  • EP6-A, Evaluation of the Linearity of Quantitative Measurement Procedures: A Statistical Approach; Approved Guideline
  • EP9-A, Method Comparison and Bias Estimation using Patient Samples; Approved Guideline
  • EP12-A, User Protocol for Evaluation of Qualitative Test Performance--Approved Guideline
  • C28-A2, How to Define and Determine Reference Intervals in the Clinical Laboratory; Approved Guideline
  • GP10-A, Assessment of the Clinical Accuracy of Laboratory Tests using Receiver Operating Characteristic (ROC) Plots; Approved Guideline
  • EP10-A, Preliminary Evaluation of Clinical Chemistry Methods; Approved Guideline
  • EP7-A, Interference Testing in Clinical Chemistry--Approved Guideline

System Requirements

Category Requirements
Operating Systems
  • Windows XP (32-bit)
  • Windows 7 (32-bit and 64-bit)
  • Windows Server 2008 (64-bit)
  • Windows 8.1 (EE 11.2 only)(64-bit)
  • Windows Server 2012R2 (EE11.2 only) (64-bit)
System Memory
  • A minimum of 128 MB of RAM for the application
Storage
  • Minimum of 200 MB for non-network, single user implement
  • Minimum of 1 GB for networked, multi-user implementation
Other
  • Monitor (1024 x 768 minimum resolution)
  • Keyboard and Mouse
  • Local or Networked Printer
  • Adobe Acrobat Reader or compatible program