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CLSI H30-A2-2001

CLSI H30-A2-2001

$48.10

Procedure for the Determination of Fibrinogen in Plasma

Published By Publication Date Number of Pages
CLSI 2001-11-01 35
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This document provides general guidelines for performing the fibrinogen assay in the clinical laboratory. It also includes reporting of results and in vivo and in vitro conditions that may alter results. (See related publication H21-A3 in this section.)

The U.S. Food and Drug Administration (FDA) has evaluated and recognized this approved-level consensus guideline for use in satisfying a regulatory requirement.

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CLSI H30-A2-2001
$48.10