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.
Presentation of a Manufacturer's Risk Mitigation Information for Users of In Vitro Diagnostic Devices; Proposed Guideline, EP22PE
$140.00 $281.60
Performance Standards for Antimicrobial Susceptibility Testing; Twentieth Informational Supplement, M100S20
$127.00 $254.75
Specimen Labels: Content and Location, Fonts, and Label Orientation; Proposed Standard, AUTO12P
$146.00 $292.58
Sweat Testing: Sample Collection and Quantitative Chloride Analysis; Approved Guideline - Third Edition, C34A3E
$90.00 $180.00