ISO 9000:2005
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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Quality management systems — Fundamentals and vocabulary
Hardcopy , PDF
English, Spanish, Castilian, French, Russian
20-09-2005
30-03-2025
ISO 9000:2005 describes fundamentals of quality management systems, which form the subject of the ISO 9000 family, and defines related terms.
It is applicable to the following:
a) organizations seeking advantage through the implementation of a quality management system;
b) organizations seeking confidence from their suppliers that their product requirements will be satisfied;
c) users of the products;
d) those concerned with a mutual understanding of the terminology used in quality management (e.g. suppliers, customers, regulators);
e) those internal or external to the organization who assess the quality management system or audit it for conformity with the requirements of ISO 9001 (e.g. auditors, regulators, certification/registration bodies);
f) those internal or external to the organization who give advice or training on the quality management system appropriate to that organization;
g) developers of related standards.
| Committee |
ISO/TC 176/SC 1
|
| DocumentType |
Standard
|
| Pages |
30
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| EN ISO 9000:2005 | Identical |
| AS/NZS ISO 9000:2006 | Identical |
| BS EN ISO 9000:2005 | Identical |
| UNE-EN ISO 9000:2005 | Identical |
| JIS Q 9000:2006 | Identical |
| CLSI M52:2010(R2020) | Verification of Commercial Microbial Identification and Antimicrobial Susceptibility Testing Systems |
| ISO 14937:2009 | Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
| ISO/IEC TR 24774:2010 | Systems and software engineering — Life cycle management — Guidelines for process description |
| ISO 3534-2:2006 | Statistics — Vocabulary and symbols — Part 2: Applied statistics |
| IEC 62507-1:2010 | Identification systems enabling unambiguous information interchange - Requirements - Part 1: Principles and methods |
| JEDEC JESD 670 A:2013 | QUALITY SYSTEM ASSESSMENT |
| I.S. EN ISO 11135:2014&A1:2019/LC:2019 | Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1: Revision of Annex E, Single batch release (ISO 11135:2014/Amd 1:2018)<br> |
| I.S. EN ISO 11137-1:2015/A2:2019 | Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 2: Revision to 4.3.4 and 11.2 (ISO 11137- 1:2006/Amd 2:2018) |
| CLSI MM19 A : 1ED 2011 | ESTABLISHING MOLECULAR TESTING IN CLINICAL LABORATORY ENVIRONMENTS |
| CSA IEC 62366-1:15 (R2020) | Medical devices — Part 1: Application of usability engineering to medical devices (Adopted IEC 62366-1:2015, first edition, 2015-02) | Dispositifs médicaux — Partie 1 : Application de l’ingénierie de l’aptitude à l’utilisation aux dispositifs médicaux (norme IEC 62366-1:2015 adoptée, première édition, 2015-02) |
| ASME B16.36:2020 | Orifice Flanges |
| INCITS/ISO TS 19159-1 : 2014(R2025) | Geographic information -- Calibration and validation of remote sensing imagery sensors and data -- Part 1: Optical sensors, a Technical Report prepared by INCITS and registered with ANSI |
| CSA ISO 14044:06 (R2021) | Environmental management - Life cycle assessment - Requirements and guidelines (Adopted ISO 14044:2006, first edition, 2006-07-01) |
| INCITS/ISO/IEC 29109-1:2009(R2020) | Information technology - Conformance testing methodology for biometric data interchange formats defined in ISO/IEC 19794 - Part 1: Generalized conformance testing methodology |
| INCITS/ISO/IEC 27036-1:2014(2019) | Information technology -- Security techniques -- Information security for supplier relationships -- Part 1: Overview and concepts |
| API RP 5EX:2018(R2024) | Design, Verification, and Application of Solid Expandable Systems |
| AS ISO 14044:2019 | Environmental management - Life cycle assessment - Requirements and guidelines |
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