2014, 290 pages, 6 x 9 perfect-bound
ISBN13: 978-1-886958-28-9
ISBN 1-886958-28-9
Download a free TOC and excerpt of the book
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 I really need 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. Implementing 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 |