CLSI eNews - 1 December 2006  (Plain Text Version)

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News
 Executive Vice President's Message
 CDC Cooperative Agreement: CLSI Advances Vision of Global Growth and Mission to Improve Health Care Worldwide
 Essential New CLSI Antimicrobial Susceptibility Testing Updates Scheduled for Release in January 2007
 Following the Rules: CLSI Auto10-A document provides a pathway to increased quality and efficiency
 CLSI Announces New Corresponding and Associate Active Membership Categories Effective 1 January 2007
 Press Releases
Standards Status
 ALERT: Proposed-level Document Voting Period Reduced to 60 days
 Vote and Deadlines
 Recently Approved Documents
Events and Exhibits
 Upcoming Events
 CLSI Meetings Calendar
Participate in CLSI
 Volunteer
 New and Sustaining Members
 Update Your Subscription


Recently Approved Documents

Autoverification of Clinical Laboratory Test Results (AUTO10-A); IT Security of In Vitro Diagnostic Instruments and Software Systems (AUTO11-A); Preliminary Evaluation of Quantitative Clinical Laboratory Measurement Procedures (EP10-A3); Viral Culture (M41-A)

EP10-A3Preliminary Evaluation of Quantitative Clinical Laboratory Measurement Procedures; Approved Guideline—Third Edition
This guideline provides experimental design and data analysis for preliminary evaluation of the performance of a measurement procedure or device.
Purchase here.

M41-AViral Culture; Approved Guideline
This document provides guidance for viral culture and identification procedures performed in the clinical virology laboratory.
Purchase here.

Second Notice

AUTO10-AAutoverification of Clinical Laboratory Test Results; Approved Guideline
This document provides a general framework that will allow each laboratory to easily design, implement, validate, and customize rules for autoverification (automated verification) based on the needs of its own patient population.
Purchase here.

AUTO11-AIT Security of In Vitro Diagnostic Instruments and Software Systems; Approved Standard
This document provides a framework for communication of IT security issues between the IVD system vendor and the healthcare organization.
Purchase here.


Our procedures have been designed to ensure that consensus has been achieved when a standard or guideline is published at the approved level. This means that a document has been rigorously reviewed by the authoring subcommittee, the area committee overseeing the project, the Board of Directors, and the medical-testing community that participates in the consensus process by carefully reviewing and commenting on the standard or guideline.

You may automatically receive or select approved-level documents as a member benefit.  Find out more about joining CLSI:  view membership options and benefits.


For more information or to contact us directly, please visit www.clsi.org l ©2006 Clinical and Laboratory Standards Institute