ISO 15189:2003 – Quality management, evaluation and continual improvement

Author:

Burnett David

Abstract

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.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

Reference7 articles.

1. ISO 15189:2003. Medical laboratories − particular requirements for quality and competence.

2. ISO/IEC 17025:1999. General requirements for the competence of testing and calibration laboratories.

3. ISO 9001:2000. Quality management systems − requirements.

4. Clinical Pathology Accreditation (UK). Standards for the Medical Laboratory (www.cpa-uk.co-uk).

5. Burnett D. A practical guide to accreditation in laboratory medicine. London: ACB Venture Publications, 2002 (www.acb.org.uk).

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