Draft
International Standard
ISO/DIS 22367
Medical laboratories — Application of risk management to medical laboratories
Reference number
ISO/DIS 22367
Edition 2
Проект Международный стандарт
Preview
ISO/DIS 22367
87738
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Проект данного международного стандарта находится на этапе рассмотрения членами ИСО.
Текущее издание: ISO 22367:2020

ISO/DIS 22367

ISO/DIS 22367
87738
Язык
Формат
CHF 65
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Тезис

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.

The requirements of this document are applicable to all aspects of the examinations and services of a medical laboratory, including the pre-examination and post-examination aspects, examinations, accurate transmission of test results into the electronic medical record and other technical and management processes described in ISO 15189.

This document does not specify acceptable levels of risk.

This document does not apply to risks from post-examination clinical decisions made by healthcare providers.

This document does not apply to the management of risks affecting medical laboratory enterprises that are addressed by ISO 31000, such as business, economic, legal, and regulatory risks.

Общая информация

  •  : В стадии разработки

    You can help develop this draft international standard by contacting your national member

    : Начало голосования по проекту между-народно-го стандарта: 3 мес. [40.20]
  •  : 2
  • ISO/TC 212
    11.100.01 
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