Quality Management Evaluation for Tobacco Commercial Enterprises in Shandong Province Based on Factor-Clustering Method

Author(s):  
Wenwen Wang ◽  
Ren Xiaoling
2019 ◽  
Vol 14 (4) ◽  
pp. 238-258
Author(s):  
Leander Luiz Klein ◽  
Mirela Schramm Tonetto Correio

2014 ◽  
Vol 30 (2) ◽  
pp. 180-184
Author(s):  
Yunna Wu ◽  
Yong Huang ◽  
Shuo Zhang ◽  
Yan Zhang

Author(s):  
David Burnett

AbstractThe requirements of ISO 15189:2003 are discussed in the context of a process- and outcome-based quality management model in which the user's needs are the central focus. The requirements of ISO 15189:2003 are examined in terms of organisation and a quality management system, stressing the importance of evidence, document control, and control of records and clinical material. Examples are provided from the areas of resource management, and pre-examination, examination and post-examination processes. In the final section the importance of evaluation and continual improvement is presented in relation to internal audit and external assessment, non-conformity, corrective and preventative action and management review.


Author(s):  
Petros Karkalousos

The new version of the ?SO 15189:2007 Standard was published in 2012, and it is called ISO 15189:2012. The new version is more specific to clinical laboratories as compared to the old one. The present chapter emphasizes in the most important changes between the two versions of the standard, especially in those that reveal the “spirit” of the new version. Some of these refer to ethics, quality management system, encouragement of the staff, risk management, evaluation of staff performance, purchase and withdraw of equipment, laboratory facilities, reagents and consumables, communication between the laboratory and its stakeholders, verification of the results by trained personnel, procedures of reporting the results, metrological procedures and traceability, function of laboratory information system, and responsibilities of laboratory director.


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