• CLSI QMS06 A3 : 3ED 2011

    Current The latest, up-to-date edition.

    QUALITY MANAGEMENT SYSTEM: CONTINUAL IMPROVEMENT

    Available format(s):  Hardcopy, PDF

    Language(s):  English

    Published date:  30-06-2011

    Publisher:  Clinical Laboratory Standards Institute

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    Table of Contents - (Show below) - (Hide below)

    Abstract
    Committee Membership
    Foreword
    1 Scope
    2 Introduction
    3 Terminology
    4 Continual Improvement: Common Supporting Elements
    5 Continual Improvement: Fundamental Processes
    6 Conclusion
    References
    Additional References
    Appendix A - Quality Report Template by Quality Indicator
    Appendix B - Quality Report Template by Quality System
                 Essential
    Appendix C - Plan-Do-Check-Act Example
    Appendix D - Plan-Do-Check-Act Template
    Appendix E - Decision Matrix - Opportunity for Improvement
                 Prioritization Example
    Appendix F - Decision Matrix - Prioritization Template
    Appendix G - Failure Modes, Effects, and Criticality Analysis
                 (FMECA) Template
    Appendix H - Workplace Audit Template
    Appendix I - 5S Plus Audit Template
    Appendix J - Customer Survey Example
    Appendix K - Waste Walk Observation Template
    Appendix L - Management Review Meeting Agenda Example
    Appendix M - Management Review Meeting Record Example
    Appendix N - Continual Improvement Team Meeting agenda
                 Template
    Appendix O - Meeting Record Template
    Appendix P - Document Change Request Form Template
    Appendix Q - Risk Management Plan Elements and File Elements
    Appendix R - Communication Plan Example
    Appendix S - Examples of Laboratory Quality Indicators
    Appendix T - Sample Data Presentation for Key Performance
                 Indicators
    Appendix U - Laboratory Scorecard Examples
    Appendix V - Continual Improvement Charter Template
    Appendix W - Implementation Plan Template
    Appendix X - Sample Turnaround Time Reduction
                 Implementation Plan
    Appendix Y - Evaluation Report Template
    Appendix Z - Control Plan Template
    Appendix AA - Close-Out Plan Template
    The Quality Management System Approach
    Related CLSI Reference Materials

    Abstract - (Show below) - (Hide below)

    Covers written and graphic descriptions of the fundamental processes and common supporting elements in a continual improvement (CI) program.

    Scope - (Show below) - (Hide below)

    This guideline includes written and graphic descriptions of thefundamental processes and common supporting elements in a continualimprovement (CI) program. It provides the user with definitions, concepts,methods, and tools for implementing an effective program and meetingapplicable requirements. The CI fundamental processes include thefollowing:Identifying opportunities for improvement (OFIs)Selecting an opportunityGenerating solution(s)Implementing solution(s)Evaluating effect of solution(s)Integrating and sustaining improvement(s)The CI common supporting elements include, but are not limited to:Management reviewTeamworkImprovement models and toolsDocuments and recordsChange managementRisk managementCommunicationThis guideline is intended for use by all organizations and individualsinvolved in the management or execution of preexamination, examination,and postexamination phases of the medical laboratory. This documentmay be applicable to other laboratories and nonlaboratory settings.This guideline is not meant to be prescriptive nor a comprehensiveinstructional manual for using the tools described. It does not addresscontent and detail covered in other CLSI documents nor requirementsspecific to any regulatory or accrediting organization.

    General Product Information - (Show below) - (Hide below)

    Development Note Supersedes NCCLS GP22 A2. (07/2011) Formerly CLSI GP22 A3. (07/2013)
    Document Type Miscellaneous Product
    Publisher Clinical Laboratory Standards Institute
    Status Current
    Supersedes

    Standards Referenced By This Book - (Show below) - (Hide below)

    CLSI MM9 A2 : 2ED 2014 NUCLEIC ACID SEQUENCING METHODS IN DIAGNOSTIC LABORATORY MEDICINE
    CLSI QMS25 : 1ED 2016 HANDBOOK FOR DEVELOPING A LABORATORY QUALITY MANUAL
    CLSI QMS20 R : 1ED 2014 UNDERSTANDING THE COST OF QUALITY IN THE LABORATORY
    CLSI MM3 A3 : 3ED 2015 MOLECULAR DIAGNOSTIC METHODS FOR INFECTIOUS DISEASES
    CLSI QMS17 : 2017 EXTERNAL ASSESSMENTS, AUDITS, AND INSPECTIONS OF THE LABORATORY
    CLSI QMS11 : 2ED 2015 NONCONFORMING EVENT MANAGEMENT
    UNE-EN ISO 15189:2013 Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)
    CLSI QMS19 : 2017 CUSTOMER FOCUS IN A QUALITY MANAGEMENT SYSTEM
    CLSI QMS18 : 1ED 2015 PROCESS MANAGEMENT
    DIN EN ISO 15189:2014-11 Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)
    CLSI QMS24 : 3ED 2016 USING PROFICIENCY TESTING AND ALTERNATIVE ASSESSMENT TO IMPROVE MEDICAL LABORATORY QUALITY
    CLSI QMS01 A4 : 4ED 2011 QUALITY MANAGEMENT SYSTEM: A MODEL FOR LABORATORY SERVICES
    CLSI C57 : 1ED 2015 MASS SPECTROMETRY FOR ANDROGEN AND ESTROGEN MEASUREMENTS IN SERUM
    CLSI POCT4 : 3ED 2016 ESSENTIAL TOOLS FOR IMPLEMENTATION AND MANAGEMENT OF A POINT-OF-CARE TESTING PROGRAM
    CLSI GP47 : 1ED 2015 MANAGEMENT OF CRITICAL- AND SIGNIFICANT-RISK RESULTS
    CLSI GP41 : 7ED 2017 COLLECTION OF DIAGNOSTIC VENOUS BLOOD SPECIMENS

    Standards Referencing This Book - (Show below) - (Hide below)

    CLSI QMS12 A : 1ED 2010 DEVELOPMENT AND USE OF QUALITY INDICATORS FOR PROCESS IMPROVEMENT AND MONITORING OF LABORATORY QUALITY
    CLSI QMS01 A4 : 4ED 2011 QUALITY MANAGEMENT SYSTEM: A MODEL FOR LABORATORY SERVICES
    CLSI QMS11 A : 1ED 2007 MANAGEMENT OF NONCONFORMING LABORATORY EVENTS
    CLSI QMS03 A3 : 3ED 2009 TRAINING AND COMPETENCE ASSESSMENT
    CLSI GP2 A5 : 5ED 2006 LABORATORY DOCUMENTS - DEVELOPMENT AND CONTROL
    CLSI EP18 A2 : 2ED 2009 RISK MANAGEMENT TECHNIQUES TO IDENTIFY AND CONTROL LABORATORY ERROR SOURCES
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