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PDF EP23-A : Laboratory Quality Control Based on Risk Management

Setting the standard for quality in medical laboratory testing around the world The Clinical and Laboratory Standards Institute (CLSI) is a not-for-profit membership organization that brings together the varied perspectives and expertise of the worldwide laboratory community for the advancement of a common cause: to foster excellence in laboratory

PDF CLSI EP23-A Laboratory Quality Control Based on Risk

Feb 14 2012 · EP23 – “The Right QC” • EP23 helps the lab director and the lab staff better understand their entire testing process from collecting the sample to reporting the result • EP23 stresses the importance of identifies and formalizes all of the other activities that labs do to ensure quality results

  • Where can I find a ep23 workbook?

    This document is available in electronic format only. You may also be interested in... Buy EP23 Workbook, A Practical Guide for Laboratory Quality Control Based on Risk Management, at CLSI. Find more standards documents in the CLSI Shop.

  • What is ep23-a?

    EP23-A addresses the clinical laboratory path of workflow steps indicated by an “X.” For a description of the document listed in the grid, please refer to the Related CLSI Reference Materials section on the following page. SAM

  • What is the CLSI consensus process?

    CLSI documents undergo periodic evaluation and modification to keep pace with advancements in technologies, procedures, methods, and protocols afecting the laboratory or health care. CLSI’s consensus process depends on experts who volunteer to serve as contributing authors and/or as participants in the reviewing and commenting process.

  • What does CLSI stand for?

    Clinical and Laboratory Standards Institute (CLSI). Laboratory Quality Control Based on Risk Management; Approved Guideline. CLSI document EP23-A (ISBN 1-56238-767-7 [Print]; ISBN 1-56238-768-5 [Electronic]). Clinical and Laboratory Standards Institute, 950 West Valley Road, Suite 2500, Wayne, Pennsylvania 19087 USA, 2011.

Clinical and Laboratory Standards Institute

Setting the standard for quality in medical laboratory testing around the world. The Clinical and Laboratory Standards Institute (CLSI) is a not-for-profit membership organization that brings together the varied perspectives and expertise of the worldwide laboratory community for the advancement of a common cause: to foster excellence in laboratory

Consensus Process

Consensus—the substantial agreement by materially afected, competent, and interested parties—is core to the development of all CLSI documents. It does not always connote unanimous agreement, but does mean that the participants in the development of a consensus document have considered and resolved all relevant objections and accept the resulting ag

Commenting on Documents

CLSI documents undergo periodic evaluation and modification to keep pace with advancements in technologies, procedures, methods, and protocols afecting the laboratory or health care. CLSI’s consensus process depends on experts who volunteer to serve as contributing authors and/or as participants in the reviewing and commenting process. At the end o

Laboratory Quality Control Based on Risk Management; Approved Guideline

James H. Nichols, PhD, DABCC, FACB Ronald H. Laessig, PhD Wadid Sadek, PhD Sousan S. Altaie, PhD Ronalda Leneau, MS, MT(ASCP) Mitchell G. Scott, PhD Greg Cooper, CLS, MHA Jacob (Jack) B. Levine, MBA Ann E. Snyder, MT(ASCP) Paul Glavina W. Gregory Miller, PhD Liz Walsh, CLS, NCA Abdel-Baset Halim, PharmD, PhD, DABCC Robert Murray, JD, PhD Gitte Wenn

Introduction

In this document, you will learn how to create a quality control plan (QCP) that is customized for your institution, facility, and laboratory, run your tests in an effective and efficient manner, so that you can improving patient care. clsi.org

You will learn:

How to compile information into How to determine if potential errors clsi.org

Laboratory Quality Control Based on Risk Management; Approved Guideline

note: This document may not satisfy the requirements of all regulatory, accreditation, or certification bodies. clsi.org

Laboratories need to comply with all applicable requirements

in the development of their QCPs. Scope This document describes good laboratory practice for developing and maintaining a QCP for medical laboratory testing using internationally recognized risk management principles. An individual QCP should be established, maintained, and modified as needed for each measuring system. The QCP is based on the perfo

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