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ISO 15190

Medical laboratories — Requirements for safety

active, Most Current
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Organization: ISO
Publication Date: 1 February 2020
Status: active
Page Count: 88
ICS Code (Laboratory medicine in general): 11.100.01
scope:

This document specifies requirements for safe practices in the medical laboratory (herein after referred to as "the laboratory").

Document History

ISO 15190
February 1, 2020
Medical laboratories — Requirements for safety
This document specifies requirements for safe practices in the medical laboratory (herein after referred to as “the laboratory”).
ISO 15190
October 15, 2003
Medical laboratories Requirements for safety
A description is not available for this item.

References

This document references:
CLSI QMS04 - Laboratory Design
Published by CLSI on June 1, 2016
This guideline discusses selected elements of laboratory design that affect the planning, layout, and safety of the medical laboratory. These elements include space, workflow, casework, equipment,...
This document references:
EN ISO 22367 - Medical laboratories - Application of risk management to medical laboratories
Published by CEN on March 1, 2020
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...
This document references:
Z9.5 - Laboratory Ventilation
Published by AIHA on January 1, 2012
Every laboratory will benefit from this outline of laboratory ventilation requirements and practices. Chapters include performance tests, air cleaning, preventive maintenance, and work practices....
This document references:
BS 6324-1 - Terms relating to surgical implants — Part 1: Glossary of general medical terms
Published by BSI on January 31, 1984
A description is not available for this item.
This document references:
EN 12469 - Biotechnology - Performance Criteria for Microbiological Safety Cabinets
Published by CEN on May 1, 2000
A description is not available for this item.
This document references:
EN ISO 22367 - Medical laboratories - Application of risk management to medical laboratories
Published by CEN on March 1, 2020
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...
This document references:
CLSI QMS04 - Laboratory Design
Published by CLSI on June 1, 2016
This guideline discusses selected elements of laboratory design that affect the planning, layout, and safety of the medical laboratory. These elements include space, workflow, casework, equipment,...
This document is referenced by:
ISO 22367 - Medical laboratories — Application of risk management to medical laboratories
Published by ISO on February 1, 2020
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...
This document is referenced by:
BS EN ISO 18113-1 - In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) -Part 1: Terms, definitions and general requirements
Published by BSI on October 31, 2011
A description is not available for this item.
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