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基本的质量管理体系

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A new reference on Quality Management Systems, addressing both management and technical requirements of quality systems for medical laboratories.
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2014, 290 pages, 6 x 9 perfect-bound
ISBN13: 978-1-886958-28-9
ISBN 1-886958-28-9

written by James O. Westgard, PHD and Sten Westgard, MS
With contributions from Leo Serrano, MS, FACHE, Cheryl Wildermuth, MS MT(ASCP), Gabriel Migliarino, PhD, and Evangelina Hernandez, MS

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Compliance is no longer enough

It's become clear in the US that the CLIA final rules set too low a bar. For laboratories that want to compete, thrive, and distinguish themselves from their competition, they need to strive for a higher level of quality. A Quality Management System is the next level of quality that differentiates the best labs from the rest of the pack.

What's a laboratory to do?

In this vital new manual, Dr. James O. Westgard, sorts through all the ISO standards, CLSI guidelines, WHO and CDC recommendations, as well as the trends and fads, distilling Quality Management Systems into something less fuzzy and more concrete. With practical step-by-step directions, laboratories can begin their QMS journey immediately

Here are just some of the topics covered:

So do Ireallyneed to understand Quality Management Systems?

Rather than making an uncoordinated set of attempts to assure quality, the Quality Management System unifies, systematizes, and standardizes Quality in the medical laboratory. It heightens Quality Management to the level of organizational culture. It ingrains the correct practices into the entire staff. While this seems like a tall order, Dr. Westgard shows practical ways to implement indicators, checklists, and benchmarks to achieve this level of quality.


Table of Contents

I: Basic Quality Management Systems for Regulation and Accreditation
1. Understanding Quality Management Systems 1
2. Reviewing QMS Essentials 11
3. Focusing on ISO 15189 23
4. Preparing for QMS Implementation 37
5.实现g Management Requirements 59
6. Implementing Technical Requirements 79
7. A Lab's Journey to CAP-ISO 15189 Accreditation 95
II. Six Sigma Quality Management Systems for Examination Procedures
8. Developing a Scientific Quality System 107
9. Defining Quality for Intended Use 131
10. Selecting an Examination Procedure 145
11. Validating Performance of an Examination Procedure 159
12. Defining Statistical QC Procedures 171
13. Formulating Total Quality Control Plans 189
14. Monitoring Nonconformities 207
15. Measuring the Uncertainty of Measurements 223
16. Managing Quality in the Real World 239
17. Improving Quality in the Real World 245
Index 285
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