CLSI eNews - 1 June 2007 (Plain Text Version)

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Executive Vice President's Message
CLSI Participates in Open House for Sub-Saharan Africa Standards Leaders
Join Us for a Series of Live Web Broadcasts
Standardization for medical laboratory testing, including in vitro diagnostic test systems
Flow Cytometry: New Guidelines to Support Its Clinical Application
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Recently Distributed ISO Standards
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Standardization for medical laboratory testing, including in vitro diagnostic test systems

by René Dybkaer, James H. Jorgensen, Donald M. Powers and Klaus E. Stinshoff

In memory of Desmond Kenny, Convenor of Working Group 1 of ISO/TC 212, who died on 18 December 2006.

ISO/TC 212 was established in 1995 to promote quality and safety in medical laboratory testing and develop International Standards for medical laboratories and in vitro diagnostic (IVD) manufacturers. The scope of TC 212 is comprised of WG 1, Quality and competence in the medical laboratory; WG 2, Reference systems ; WG 3, In vitro diagnostic products ; and WG 4, Antimicrobial susceptibility testing.

Read the full article text as published in ISO Focus, Volume 4, No. 2, February 2007, ISSN 1729-8709.