EP Evaluator

TThe Standard for Quality Assurance software designed to evaluate and measure the clinical laboratory performance and provides clear, concise, 'inspector-ready' reports meeting all CLIA, 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 the leading instrument and method validation software package in the in vitro industry.



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Version Comparisons

 
Regulatory Requirements
EP Evaluator Versions
 
CLIA
CAP
TJC
COFRAC
Single Standard
Network Standard
Single Pro
Network Pro
Features
Concurrent, Multiple User Access
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Composite Reporting
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Project Management
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Import Data from Middleware (ODBC)
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Security Audit Trail
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User Accounts for Network Security
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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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CLSI EP9-A3 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 Method Comparison
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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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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 and up) (64-bit)
  • Windows Server 2012R2 (EE11.2 and up) (64-bit)
  • Windows 10 (EE11.3 and up)
  • Server 2016
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