This document contains guidelines for specimen collection, blood film preparation, and staining procedures. Recommendations for optimum timing of specimen collection to assist laboratories in detecting, identifying and reporting certain parasites are also included.
The U.S. Food and Drug Administration (FDA) has evaluated and recognized this approved-level consensus guideline for use in satisfying a regulatory requirement.
More CLSI standard pdf
CLSI H60-A (R2019)
Laboratory Testing for the Lupus Anticoagulant; Approved Guideline, H60AE
$90.00 $180.00
CLSI H52-A2 (R2016)
Red Blood Cell Diagnostic Testing Using Flow Cytometry; Approved Guideline - Second Edition, H52A2E
$90.00 $180.00
CLSI EP10-A3-AMD (R2019)
Preliminary Evaluation of Quantitative Clinical Laboratory Methods, Approved Guideline - Third Edition, EP10A3AMDE
$90.00 $180.00
CLSI MM22-A
Microarrays for Diagnosis and Monitoring of Infectious Diseases; Approved Guideline, MM22AE
$90.00 $180.00