: Assesses within-run and total precision over multiple days to ensure consistent results.
The release of version 12 introduced several critical updates designed to align with modern Clinical and Laboratory Standards Institute (CLSI) guidelines and improve integration with lab middleware.
is a comprehensive laboratory quality assurance (QA) software suite developed by Data Innovations to automate instrument performance verification and regulatory compliance. It is widely recognized as the industry standard for clinical laboratories needing to meet CLIA, CAP, and The Joint Commission requirements. Key Enhancements in EP Evaluator 12 ep evaluator 12
: A major enhancement that allows for more flexible method comparison. It supports up to five replicates per instrument for each specimen, significantly improving precision and reducing random bias errors.
: Evaluates the agreement between two instruments or methods using Deming or Passing-Bablok regression. : Assesses within-run and total precision over multiple
: By automating complex statistical analysis, labs can free up staff to focus on patient testing rather than manual data entry and spreadsheet calculations.
: Helps labs verify or establish "normal ranges" for specific patient populations. It is widely recognized as the industry standard
: Ensures compliance with 21 CFR Part 11 for electronic records and audit trails, which is vital for maintaining accreditation.
: Aligns with the CLSI EP6-A standard to verify that an assay performs accurately across its entire measurable range.
: Provides a consistent, vendor-neutral platform for evaluating all instruments across a health system, regardless of the manufacturer.