Your shopping cart is empty!
Clinical and Laboratory Standards Institute, 09/20/2001
Publisher: CLSI
File Format: PDF
$90.00$180.00
Published:20/09/2001
Pages:46
File Size:1 file , 1.8 MB
Note:This product is unavailable in Russia, Belarus
This guideline outlines specimen requirements; performance criteria; algorithms for the potential use of sequential or duplicate testing; recommendations for intermethod comparisons of immunological test kits for detecting infectious diseases; and specifications for development of reference materials.This document is no longer being reviewed as part of the CLSI consensus process. However, because of its usefulness to a limited segment of the healthcare community, CLSI is continuing to make the document available for its informational content.
This document is available in electronic format only.
Specification for Low-Level Protocol to Transfer Messages Between Clinical Laboratory Instruments and Computer Systems; Approved Standard-Second Edition, LIS01A2E
$101.00 $202.39
Detection of HLA-Specific Alloantibody by Flow Cytometry and Solid Phase Assays, Proposed Guideline, ILA29AE
$90.00 $180.00
User Protocol for Evaluation of Qualitative Test Performance; Approved Guideline, Second Edition, EP122A
Collection, Transport, and Processing of Blood Specimens for Testing Plasma-Based Coagulation Assays; Approved Guideline, Fifth Edition, H21-A5