<p><span lang="EN-GB">This document specifies a process for a medical laboratory to identify and manage the risks to patients, laboratory workers and service providers that are associated with medical laboratory examinations. The process includes identifying, estimating, evaluating, controlling and monitoring the risks.</span></p>
<p><span lang="EN-GB">The requirements of this document are applicable to all aspects of the examinations and services of a medical laboratory, including the pre-examination, examination, and post-examination aspects including accurate transmission of examination results into the electronic medical record, as well as other technical and management processes described in ISO 15189.</span></p>
<p><span lang="EN-GB">This document does not specify acceptable levels of risk.</span></p>
<p><span lang="EN-GB">This document does not apply to risks from post-examination clinical decisions made by healthcare providers.</span></p>
<p><span lang="EN-GB">This document complements the management of risks affecting medical laboratory enterprises that are addressed by ISO 31000, such as business, economic, legal, and regulatory risks.</span></p>
Registration number (WIID)
87738
Scope
<p><span lang="EN-GB">This document specifies a process for a medical laboratory to identify and manage the risks to patients, laboratory workers and service providers that are associated with medical laboratory examinations. The process includes identifying, estimating, evaluating, controlling and monitoring the risks.</span></p>
<p><span lang="EN-GB">The requirements of this document are applicable to all aspects of the examinations and services of a medical laboratory, including the pre-examination, examination, and post-examination aspects including accurate transmission of examination results into the electronic medical record, as well as other technical and management processes described in ISO 15189.</span></p>
<p><span lang="EN-GB">This document does not specify acceptable levels of risk.</span></p>
<p><span lang="EN-GB">This document does not apply to risks from post-examination clinical decisions made by healthcare providers.</span></p>
<p><span lang="EN-GB">This document complements the management of risks affecting medical laboratory enterprises that are addressed by ISO 31000, such as business, economic, legal, and regulatory risks.</span></p>
