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IEC/TR 80002 Medical device software IEC/TR 80002-1:2009 Part 1: Guidance on the application of ISO 14971 to medical device software; ISO/TR 80002-2:2017 Part 2: Validation of software for medical device quality systems; IEC/TR 80002-3:2014 Part 3: Process reference model of medical device software life cycle processes
ISO/IEC TR 8802-1:2001 Part 1: Overview of Local Area Network Standards; ISO/IEC/IEEE 8802-1Q:2016 Part 1Q: Bridges and bridged networks; ISO/IEC/IEEE 8802-1X:2013 Part 1X: Port-based network access control; ISO/IEC/IEEE 8802-1AB:2017 Part 1AB: Station and media access control connectivity discovery
ISO 8000 is being developed by ISO technical committee TC 184, Automation systems and integration, sub-committee SC 4, Industrial data. Like other ISO and IEC standards, ISO 8000 is copyrighted and is not freely available. [7] Parts 1, 2 and 8 are ISO horizontal deliverables, identifying them as applicable to all sectors.
1 ISO 1 – ISO 19999. 2 ISO 20000 – ISO 99999. 3 See also. 4 Notes. 5 References. ... Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...
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ISO 80000-8:2020 revised ISO 80000-8:2007, [37] which revised ISO 31-7:1992. [38] It gives names, symbols, definitions, and units for quantities of acoustics. The descriptive text of this part is available online. [39] It has a foreword, scope introduction, scope, normative references (of which there are none), as well as terms, and definitions.
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ISO/IEC TR 20943-1:2003 Part 1: Data elements; ISO/IEC TR 20943-3:2004 Part 3: Value domains; ISO/IEC TR 20943-5:2013 Part 5: Metadata mapping procedure; ISO/IEC TR 20943-6:2013 Part 6: Framework for generating ontologies; ISO/IEC 20944 Information technology - Metadata Registries Interoperability and Bindings (MDR-IB)