CLSI QMS18

Process Management, 2nd Edition

This guideline describes five requirements for managing laboratory processes and provides suggestions for effectively meeting regulatory and accreditation requirements, assessing process risks, optimizing efficient use of resources, and contributing to patient safety and positive outcomes.

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Chairholder: Lucia M. Berte, MA, MT(ASCP)SBB, DLM, CQA(ASQ)CMQ/OE

Date of Publication: May 31, 2023

Order Code PDF: CLSI QMS18Ed2E
ISBN Number: 978-1-68440-184-0

Order Code Print: CLSI QMS18Ed2
ISBN Number: 978-1-68440-183-3

Edition: Second

Pages: 114

CLSI QMS18 Additional Details

A guideline for global application developed through the Clinical and Laboratory Standards Institute consensus process.

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CLSI QMS18 Abstract

Clinical and Laboratory Standards Institute guideline QMS18—Process Management describes five published regulatory and accreditation requirements for management of laboratory processes. This guideline provides guidance, with explanations and examples, for meeting the five process management requirements as they apply to preexamination, examination, and postexamination processes. Because several other CLSI guidelines contain process management information for both laboratory examination and quality management processes, the examples in this guideline are for preexamination and postexamination processes.