TDS PDF

Presentation of a Manufacturer's Risk Mitigation Information for Users of In Vitro Diagnostic Devices; Proposed Guideline. Original document CLSI EP22-P-2010 in PDF format. Additional info + preview on request

Document status: Withdrawn

Laboratory Quality Control Based on Risk Management; Approved Guideline. Original standard CLSI EP23-A-2011 (2016) in PDF full version. Additional info + preview on request

Document status: Replaced by

Assessment of the Diagnostic Accuracy of Laboratory Tests Using Receiver Operating Characteristic Curves; Approved Guideline—Second Edition. Original standard CLSI EP24-A2-2011 (2016) in PDF full version. Additional info + preview on request

Document status: Active

Evaluation of Stability of In Vitro Medical Laboratory Test Reagents. Original standard CLSI EP25-Ed2-2023 in PDF full version. Additional info + preview on request

Document status: Active

Evaluation of Stability of In Vitro Diagnostic Reagents; Approved Guideline. Original standard CLSI EP25-A-2009 in PDF full version. Additional info + preview on request

Document status: Replaced by St CLSI EP25-Ed2-2023

User Evaluation of Between-Reagent Lot Variation; Approved Guideline. Original standard CLSI EP26-A-2013 in PDF full version. Additional info + preview on request

Document status: Replaced by