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BSI - BS ISO 20387

Biotechnology — Biobanking — General requirements for biobanking

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Organization: BSI
Publication Date: 31 August 2018
Status: inactive
Page Count: 46
ICS Code (Biology. Botany. Zoology): 07.080

Document History

BS EN ISO 20387
August 31, 2018
Biotechnology - Biobanking - General requirements for biobanking
A description is not available for this item.
BS ISO 20387
August 31, 2018
Biotechnology — Biobanking — General requirements for biobanking
A description is not available for this item.

References

This document references:
ISO/IEC GUIDE 99 - International vocabulary of metrology - Basic and general concepts and associated terms (VIM)
Published by ISO on January 1, 2007
In this Vocabulary, a set of definitions and associated terms is given, in English and French, for a system of basic and general concepts used in metrology, together with concept diagrams to...
This document references:
ISO/IEC 20944-1 - Information technology - Metadata Registries Interoperability and Bindings (MDR-IB) - Part 1: Framework, common vocabulary, and common provisions for conformance
Published by ISO on January 15, 2013
General ISO/IEC 20944 is a series of International Standards that describe codings, APIs, and protocols for interacting with an ISO/IEC 11179 metadata registry (MDR). This part of ISO/IEC 20944...
This document references:
ISO 17511 - In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
Published by ISO on April 1, 2020
This document specifies technical requirements and documentation necessary to establish metrological traceability of values assigned to calibrators, trueness control materials and human samples for...
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 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 17511 - In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
Published by ISO on April 1, 2020
This document specifies technical requirements and documentation necessary to establish metrological traceability of values assigned to calibrators, trueness control materials and human samples for...
This document references:
ISO/IEC 20944-1 - Information technology - Metadata Registries Interoperability and Bindings (MDR-IB) - Part 1: Framework, common vocabulary, and common provisions for conformance
Published by ISO on January 15, 2013
General ISO/IEC 20944 is a series of International Standards that describe codings, APIs, and protocols for interacting with an ISO/IEC 11179 metadata registry (MDR). This part of ISO/IEC 20944...
This document references:
ISO/IEC GUIDE 99 - International vocabulary of metrology - Basic and general concepts and associated terms (VIM)
Published by ISO on January 1, 2007
In this Vocabulary, a set of definitions and associated terms is given, in English and French, for a system of basic and general concepts used in metrology, together with concept diagrams to...
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