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H30

Procedure for the Determination of Fibrinogen in Plasma, 2nd Edition

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.)  

This document is available in electronic format only.

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Publication Details

Chairholder: Charles F. Arkin, MD

Date of Publication: November 1, 2001

ISBN Number: 1-56238-439-2

Order Code PDF: H30A2E

Order Code Print: print not available

Edition: Second

Pages: 16

H30 Additional Details

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

This document is no longer being reviewed as part of our consensus process. However, because of its usefulness to a limited segment of the healthcare community, we are continuing to make the document available for its informational content.