M36-A | Clinical Use and Interpretation of Serologic Tests for Toxoplasma gondii, 1st Edition
This guideline provides the user with information about the biology of Toxoplasma gondii, the methods available for use in the laboratory diagnosis of human toxoplasmosis, techniques that should be performed for specific clinical situations, and how to interpret laboratory results.
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.
Chairholder: Lynne S. Garcia, MS, F(AAM) Organization: LSG and Associates Date of Publication: 02/01/2004 ISBN Number: 1-56238-523-2 Edition: First Edition Pages: 23