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Abbreviations, Acronyms & Definitions
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| The table below includes the most common abbreviations, acronyms, and definitions used within the QCMD EQA programmes.
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| Glossary sections : A - C /
D - P /
Q - Z
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| QA |
Quality Assurance |
| QC |
Quality Control |
| QCMD |
Quality Control for Molecular Diagnostics |
| QM |
Quality Manual |
| QMS |
Quality Management System |
| QUALITY |
Ability of a set of inherent characteristics of a product, system or process to fulfil requirements of customers and other interested parties. |
| QUALITY ASSURANCE |
Part of quality management, focused on providing confidence that quality requirements are fulfilled. |
| QUALITY AUDIT |
A systematic and independent examination to determine whether quality activities and related results comply with planned arrangements and whether these arrangements are implemented effectively and are suitable to achieve objectives. |
| QUALITY CONTROL |
Part of quality management, focused on fulfilling quality requirements. |
| QUALITY MANAGEMENT |
That aspect of the overall management function that determines and implements the quality policy. |
| QUALITY MANAGEMENT SYSTEM |
System to establish a quality policy and quality objectives and to achieve those objectives. |
| QUALITY MANAGEMENT SYSTEM REVIEW |
A formal evaluation by top management of the status and adequacy of the Quality Management System in relation to quality policy and new objectives resulting from changing circumstances. |
| QUALITY MANUAL |
Document specifying the quality management system of an organisation. |
| QUALITY POLICY |
The overall quality intentions and direction of an organisation as regards quality, as formally expressed by top management. |
| QUALITY SYSTEM |
The organisational structure, responsibilities, procedures, processes and resources for implementing quality management. |
| SAB |
Scientific Advisory Board |
| SD |
Standard Deviation |
| SLA |
Service Level Agreement |
| SPECIFICATION |
The document that describes the requirements with which the product, material or process has to conform. |
| SUPPLIER |
The organisation that provides a product to the customer [EN ISO 8402:1995]. |
| UA |
Utility Agreement |
| VALIDATION |
Confirmation and provision of objective evidence that the requirements for a specific intended use or application have been fulfilled. |
| VERIFICATION |
The act of reviewing, inspecting, testing, checking, auditing or otherwise establishing and documenting whether items, processes, services, or documents conform to specified requirements. |
| WHO |
World Health Organisation |
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Unit 5, Technology
Terrace, Todd Campus, West of Scotland Science Park Glasgow
G20 0XA Scotland, UK
Tel: +44 (0)141 945 6474 Fax:
+44 (0)141 945 5795 Contact Us
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