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ISO 22367:2020

Medical laboratories — Application of risk management to medical laboratories
25. 2. 2020.

Опште информације

90.92     12. 9. 2023.

ISO

ISO/TC 212

Međunarodni standard

11.100.01  

engleski   španski   francuski  

Kupovina

Objavljen

Jezik na kome želite da primite dokument.

Apstrakt

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.

Životni ciklus

PRETHODNO

POVUČEN
ISO/TS 22367:2008

POVUČEN
ISO/TS 22367:2008/Cor 1:2009

TRENUTNO

OBJAVLJEN
ISO 22367:2020
90.92 Odluka o izmeni ili reviziji standarda
12. 9. 2023.

REVIDIRAN OD

PROJEKAT
ISO/FDIS 22367

Nacionalna preuzimanja

SRPS EN ISO 22367 :2020  
ISS

Medicinske laboratorije – Primena menadžmenta rizikom na medicinske laboratorije

60.60   Standard objavljen

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