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CLSI M52:2010(R2020)

Current

Current

The latest, up-to-date edition.

Verification of Commercial Microbial Identification and Antimicrobial Susceptibility Testing Systems

Available format(s)

Hardcopy

Language(s)

English

Published date

01-01-2020

$491.07
Including GST where applicable

This guideline provides recommendations for clinical laboratory professionals for verification of commercial microbial identification systems (MIS) and US Food and Drug Administration (FDA)–cleared antimicrobial susceptibility testing systems (ASTS) to fulfill regulatory or QA requirements for use in diagnostic testing.

DocumentType
Standard
ISBN
1-56238-912-2
Pages
92
PublisherName
Clinical Laboratory Standards Institute
Status
Current
Supersedes

ISO 20776-2:2007 Clinical laboratory testing and in vitro diagnostic test systems Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices Part 2: Evaluation of performance of antimicrobial susceptibility test devices
ISO 18113-1:2009 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
CLSI EP23 A : 1ED 2011 LABORATORY QUALITY CONTROL BASED ON RISK MANAGEMENT
ISO 15189:2012 Medical laboratories — Requirements for quality and competence
CLSI QMS01 A4 : 4ED 2011 QUALITY MANAGEMENT SYSTEM: A MODEL FOR LABORATORY SERVICES
ISO/IEC Guide 63:2012 Guide to the development and inclusion of safety aspects in International Standards for medical devices
CLSI M50 A : 1ED 2008 QUALITY CONTROL FOR COMMERCIAL MICROBIAL IDENTIFICATION SYSTEMS
ISO 17511:2003 In vitro diagnostic medical devices Measurement of quantities in biological samples Metrological traceability of values assigned to calibrators and control materials
ISO 9000:2005 Quality management systems Fundamentals and vocabulary
CLSI M2 A12 : 12ED 2015 PERFORMANCE STANDARDS FOR ANTIMICROBIAL DISK SUSCEPTIBILITY TESTS
CLSI LIS2 A2 : 2ED 2004 SPECIFICATION FOR TRANSFERRING INFORMATION BETWEEN CLINICAL INSTRUMENTS AND COMPUTER SYSTEMS
ISO 14971:2007 Medical devices Application of risk management to medical devices
CLSI QMS05 A2 : 2ED 2012 QUALITY MANAGEMENT SYSTEM: QUALIFYING, SELECTING, AND EVALUATING A REFERRAL LABORATORY
CLSI AUTO8 A : 1ED 2006 MANAGING AND VALIDATING LABORATORY INFORMATION SYSTEMS
CLSI M29 A4 : 4ED 2014 Protection of Laboratory Workers From Occupationally Acquired Infections<br>

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