ISO 15189:2003--quality management, evaluation and continual improvement

Clin Chem Lab Med. 2006;44(6):733-9. doi: 10.1515/CCLM.2006.126.

Abstract

The 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.

Publication types

  • Review

MeSH terms

  • Clinical Laboratory Techniques / standards*
  • Laboratories / standards*
  • Management Audit
  • Medical Errors / prevention & control
  • Quality of Health Care / trends*
  • Total Quality Management*
  • United Kingdom