CLSI M23-Ed5
Development of In Vitro Susceptibility Testing Criteria and Quality Control Parameters, 5th Edition, M23Ed5E
standard by Clinical and Laboratory Standards Institute, 01/16/2018
CLSI
Development of In Vitro Susceptibility Testing Criteria and Quality Control Parameters, 5th Edition, M23Ed5E
standard by Clinical and Laboratory Standards Institute, 01/16/2018
Quality Control for Commercially Prepared Microbiological Culture Media; Approved Standard, M22A3E
standard by Clinical and Laboratory Standards Institute, 06/20/2004
Establishing and Verifying an Extended Measuring Interval Through Specimen Dilution and Spiking, 1st Edition, EP34Ed1E
standard by Clinical and Laboratory Standards Institute, 08/13/2018
Collection, Transport, and Processing of Blood Specimens for Testing Plasma-Based Coagulation Assays; Approved Guideline, Fifth Edition, H21-A5
standard by Clinical and Laboratory Standards Institute, 01/01/2008
Standard Specification for Use of Bar Codes on Specimen Tubes in the Clinical Laboratory, LIS7AE
standard by Clinical and Laboratory Standards Institute, 04/20/2003
Management of Paper-based and Electronic Laboratory Information, 1st Edition, QMS22Ed1E
standard by Clinical and Laboratory Standards Institute, 08/01/2018
User Evaluation of Between-Reagent Lot Variation; Approved Guideline, EP26AE
standard by Clinical and Laboratory Standards Institute, 09/01/2013
Methods for Determining Bacterial Activity of Antimicrobial Agents; Approved Guideline, M26AE
standard by Clinical and Laboratory Standards Institute, 01/01/1999
Procedures for the Erythrocyte Sedimentation Rate Test; Approved Standard – Fifth Edition, H02A5
standard by Clinical and Laboratory Standards Institute, 05/01/2011
Developing and Managing a Medical Laboratory (Test) Utilization Management Program, 1st Edition, GP49Ed1E
standard by Clinical and Laboratory Standards Institute, 07/01/2017