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BSI - BS ISO 15190 - TC

Tracked Changes (Redline) - Medical laboratories — Requirements for safety

active, Most Current
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Organization: BSI
Publication Date: 12 November 2020
Status: active
Page Count: 188
ICS Code (Laboratory medicine in general): 11.100.01

Document History

BS ISO 15190 - TC
November 12, 2020
Tracked Changes (Redline) - Medical laboratories — Requirements for safety
A description is not available for this item.

References

This document references:
ISO/IEC GUIDE 63 - Guide to the development and inclusion of aspects of safety in International Standards for medical devices
Published by ISO on August 1, 2019
This document provides requirements and recommendations to writers of medical device standards on the inclusion of aspects related to safety in International Standards, based on well-established risk...
This document references:
ISO TS 20658 - Medical laboratories - Requirements for collection, transport, receipt, and handling of samples
Published by ISO on October 1, 2017
This document specifies requirements and good practice recommendations for the collection, transport, receipt and handling of samples intended for medical laboratory examinations. This document is...
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 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:
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 references:
ISO TS 20658 - Medical laboratories - Requirements for collection, transport, receipt, and handling of samples
Published by ISO on October 1, 2017
This document specifies requirements and good practice recommendations for the collection, transport, receipt and handling of samples intended for medical laboratory examinations. This document is...
This document references:
ISO/IEC GUIDE 63 - Guide to the development and inclusion of aspects of safety in International Standards for medical devices
Published by ISO on August 1, 2019
This document provides requirements and recommendations to writers of medical device standards on the inclusion of aspects related to safety in International Standards, based on well-established risk...
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