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CLSI EP30-A
Characterization and Qualification of Commutable Reference Materials for Laboratory Medicine; Approved Guideline
This document provides information to help material manufacturers in the production and characterization of commutable reference materials as well as assist assay manufacturers, proficiency testing providers, and laboratorians in the appropriate use of these materials for calibration and trueness assessment of in vitro diagnostic medical devices This document is included in the CLSI document code change and rebranding that is currently in process. The code will be changed from C53-A to EP30-A. Please make sure that the document title corresponds to the publication that you intend order
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Clinical And Laboratory Standards Institute [clsi]
Clinical And Laboratory Standards Institute [clsi]