
- 225 pages
- English
- PDF
- Available on iOS & Android
Implementing ISO/IEC 17025:2017
About this book
The focus of this book is to demystify the requirements delineated within ISO/IEC 17025: 2017, while providing a road map for organizations wishing to receive accreditation for their laboratories.AS9100, ISO 9001: 2015, and ISO 13485: 2016 are standards that have been created to support the development and implementation of effective approaches to quality management, and are recognized blueprints for the establishment of a quality management system (QMS) for many diverse industries. Similar to these recognized QMS standards, ISO/IEC 17025: 2017 for laboratory accreditation serves a unique purpose. It is not unusual for laboratories to retain dual certification in ISO 9001: 2015 and ISO/IEC 17025: 2017. However, ISO/IEC 17025: 2017 contains requirements specific to the laboratory environment that are not addressed by ISO 9001: 2015.This book highlights those differences between ISO 9001: 2015 and ISO/IEC 17025: 2017, while providing practical insight and tools needed for laboratories wishing to achieve or sustain accreditation to ISO/IEC 17025: 2017. For those currently or formerly accredited to the 2005 version of ISO/IEC 17025, an appendix outlines the changes between the 2005 and 2017 versions of the standard.
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Information
Table of contents
- Cover
- Title page
- CIP data
- Table of Contents
- List of Figures and Tables
- Acknowledgments
- Introduction
- Chapter 1 - Scope
- Chapter 2 - Normative References
- Chapter 3 - Terms and Definitions
- Chapter 4 - General Requirements
- Chapter 5 - Structural Requirements
- Chapter 6.1 - Resources Requirements: General
- Chapter 6.2 - Personnel
- Chapter 6.3 - Facilities and Environmental Conditions
- Chapter 6.4 - Equipment
- Chapter 6.5 - Metrological Traceability
- Chapter 6.6 - Externally Provided Products and Services
- Chapter 7.1 - Review of Requests, Tenders, and Contracts
- Chapter 7.2 - Selection, Verification, and Validation of Methods
- Chapter 7.3 - Sampling
- Chapter 7.4 - Handling of Test and Calibration Items
- Chapter 7.5 - Technical Records
- Chapter 7.6 - Evaluation of Measurement Uncertainty
- Chapter 7.7 - Assuring the Validity of Results
- Chapter 7.8 - Reporting the Results
- Chapter 7.9 - Complaints
- Chapter 7.10 - Nonconforming Work
- Chapter 7.11 - Control of Data and Information Management
- Chapter 8.1 - Options
- Chapter 8.2 - Management System Documentation (Option A)
- Chapter 8.3 - Control of Management System Documents (Option A)
- Chapter 8.4 - Control of Records (Option A)
- Chapter 8.5 - Actions to Address Risks and Opportunities (Option A)
- Chapter 8.6 - Improvement (Option A)
- Chapter 8.7 - Corrective Actions (Option A)
- Chapter 8.8 - Internal Audits (Option A)
- Chapter 8.9 - Management Reviews (Option A)
- Epilogue
- Appendix A - Changes between the 2005 and 2017 Versions of the Standard
- Bibliography
- Index