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BSI - BS ISO 15190

Medical laboratories — Requirements for safety

active, Most Current
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Organization: BSI
Publication Date: 31 March 2020
Status: active
Page Count: 90
ICS Code (Laboratory medicine in general): 11.100.01

Document History

BS ISO 15190
March 31, 2020
Medical laboratories — Requirements for safety
A description is not available for this item.
BS ISO 15190
November 12, 2003
Medical laboratories Requirements for safety
A description is not available for this item.

References

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 13641 - Elimination or Reduction of Risk of Infection Related to In Vitro Diagnostic Reagents
Published by CEN on May 27, 2002
A description is not available for this item.
This document references:
IEC 61010-1 - Safety requirements for electrical equipment for measurement, control, and laboratory use – Part 1: General requirements
Published by IEC on January 1, 2017
Equipment included in scope This group safety publication is primarily intended to be used as a product safety standard for the products mentioned in the scope, but shall also be used by technical...
This document references:
IEC 61010-2-040 - Safety requirements for electrical equipment for measurement, control, and laboratory use – Part 2-040: Particular requirements for sterilizers and washer-disinfectors used to treat medical materials
Published by IEC on May 1, 2020
Equipment included in scope This part of IEC 61010 specifies safety requirements for electrical equipment intended for sterilization, washing, and disinfection of medical materials in the medical,...
This document references:
ISO 35001 - Biorisk management for laboratories and other related organisations
Published by ISO on November 1, 2019
This document defines a process to identify, assess, control, and monitor the risks associated with hazardous biological materials. This document is applicable to any laboratory or other organization...
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.
This document is referenced by:
BS EN ISO 15189 + A11 - Medical laboratories - Requirements for quality and competence
Published by BSI on December 31, 2022
A description is not available for this item.
This document is referenced by:
BS ISO 14470 - Food irradiation - Requirements for the development, validation and routine control of the process of irradiation using ionizing radiation for the treatment of food
Published by BSI on January 31, 2012
A description is not available for this item.
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