Nombre | apoyo | Revisión | Disponibilidad | Fecha de emisión | Precio | ||
---|---|---|---|---|---|---|---|
PDF |
Inglés |
Vigente |
1/1/2010 |
193,00 € |
|
Detalles
This document covers portions of the life cycle of an automated multichannel hematology system and
provides guidance for validation, verification, calibration, quality assurance (QA), and quality control
(QC) through standardized approaches to ensure good laboratory science and clinical relevance. The
intended audience includes manufacturers of such devices, end-user clinical laboratories, accrediting
organizations, and regulatory bodies.
End-user clinical laboratories will also find guidance for establishment of clinically reportable intervals
(CRIs) and for QA for preexamination and examination aspects of their systems.
Información adicional
Autor | Clinical and Laboratory Standards Institute (CLSI) |
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Publicado por | CLSI |
Tipo de Documento | Norma |
Tema | /subgroups/17905 |
Fecha de confirmación | 2018-01-01 |
EAN ISBN | 1562387286 |
Reemplaza | CLSI H38P |
Palabra clave | CLSI H26-A2 (R2018) |