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INFORMATION TECHNOLOGY - METADATA REGISTRIES (MDR) - PART 6: REGISTRATION
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Available format(s): Hardcopy, PDF
Superseded date: 21-01-2017
Language(s): English
Published date: 31-12-2015
Publisher: Canadian Standards Association
ForewordIntroduction1 Scope2 Normative references3 Terms and definitions4 Concept of operation5 Metadata Registries of Administered Items6 ConformanceAnnex A (informative) - Identifiers based on ISO/IEC 6523Annex B (normative) - Contents of the Metadata Registry: Metadata attributes required for Administered ItemsAnnex C (informative) - Suggested functional operating procedures - Roles and ResponsibilitiesAnnex D (informative) - Suggested functional operating procedures - Concept of operationsAnnex E (informative) - Suggested functional operating procedures - ProceduresAnnex F (informative) - Suggested functional operating procedures - Harmonization and reuseAnnex G (informative) - Frequently Asked QuestionsBibliography
Specifies the type of information to be specified, the conditions to be met, and the procedure(s) to be followed for each metadata item to be registered in a metadata registry.
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