Outlooks on the Management System Based on ISO 17025, Applied in Acoustics and Vibration Laboratories

2015 ◽  
Vol 801 ◽  
pp. 312-316
Author(s):  
Iulian Virgil Calota

This paper is a point of view about the need and benefits of implementing of a quality management system, based on ISO 17025, in an acoustic and vibration testing laboratory. Both management and technical requirements are discussed.

2018 ◽  
Vol 26 (1) ◽  
pp. 42-48 ◽  
Author(s):  
Joanna Mytych ◽  
Mariusz J. Ligarski

Abstract The quality management systems compliant with the ISO 9001:2009 have been thoroughly researched and described in detail in the world literature. The accredited management systems used in the testing laboratories and compliant with the ISO/IEC 17025:2005 have been mainly described in terms of the system design and implementation. They have also been investigated from the analytical point of view. Unfortunately, a low number of studies concerned the management system functioning in the accredited testing laboratories. The aim of following study was to assess the management system functioning in the accredited testing laboratories in Poland. On 8 October 2015, 1,213 accredited testing laboratories were present in Poland. They investigated various scientific areas and substances/objects. There are more and more such laboratories that have various problems and different long-term experience when it comes to the implementation, maintenance and improvement of the management systems. The article describes the results of the conducted expert assessment (survey) carried out to examine the conditions for the functioning of a management system in an accredited laboratory. It also focuses on the characteristics of the accredited research laboratories in Poland. The authors discuss the selection of the external and internal conditions that may affect the accredited management system. They show how the experts assessing the selected conditions were chosen. The survey results are also presented.


2018 ◽  
Vol 31 (3) ◽  
Author(s):  
Roberta B. Carey ◽  
Sanjib Bhattacharyya ◽  
Sue C. Kehl ◽  
Larissa M. Matukas ◽  
Michael A. Pentella ◽  
...  

SUMMARY This document outlines a comprehensive practical approach to a laboratory quality management system (QMS) by describing how to operationalize the management and technical requirements described in the ISO 15189 international standard. It provides a crosswalk of the ISO requirements for quality and competence for medical laboratories to the 12 quality system essentials delineated by the Clinical and Laboratory Standards Institute. The quality principles are organized under three main categories: quality infrastructure, laboratory operations, and quality assurance and continual improvement. The roles and responsibilities to establish and sustain a QMS are outlined for microbiology laboratory staff, laboratory management personnel, and the institution's leadership. Examples and forms are included to assist in the real-world implementation of this system and to allow the adaptation of the system for each laboratory's unique environment. Errors and nonconforming events are acknowledged and embraced as an opportunity to improve the quality of the laboratory, a culture shift from blaming individuals. An effective QMS encourages “systems thinking” by providing a process to think globally of the effects of any type of change. Ultimately, a successful QMS is achieved when its principles are adopted as part of daily practice throughout the total testing process continuum.


Author(s):  
Silvia Martínez-Perales ◽  
Isabel Ortiz-Marcos ◽  
Jesús Juan Ruiz

AbstractThere is a broad consensus on the importance and advisability of testing laboratories adopting a Quality Management System (QMS) to support their work, no matter they are industrial or research oriented. However, laboratories involved in R&D have specific difficulties to implement a QMS due to the peculiar nature of their activity. This paper analyzes the main challenges and difficulties found by professionals when implementing a QMS in a research testing laboratory, based on the literature review and a questionnaire with 86 laboratories participating performed in collaboration with RedLab (Red de Laboratorios de la Comunidad de Madrid). After this analysis, a set of requirements for the competence of research testing laboratories based on ISO/IEC 17025 and UNE 166002 is defined, and an agile methodology for the fulfilment of these requirements is proposed.


2010 ◽  
Vol 46 (15) ◽  
pp. 1710-1711
Author(s):  
N. M. Konovalova ◽  
A. V. Popova

2014 ◽  
Vol 1037 ◽  
pp. 486-489
Author(s):  
Ying Ji Li ◽  
Yong Lin Wang

This paper is based on a company that manufactured the nuclear power components. This paper Studies the quality management that aimed at characteristics of multi specification and small batch production. The components which are produced at this company have been used in new energy field. Quality of nuclear power components can meet the technical requirements or not is very important to the operation and safeguard of nuclear power station in future. Group technology combined with statistical process control technology and applied in the quality management system to analyze the testing data of each working procedure in multi-kind and small-quantity production to achieve the goal of improve and control the quality of the product.


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