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The CARE Principles for Indigenous Data Governance were created to advance the legal principles underlying collective and individual data rights in the context of the [[United Nations Declaration on the Rights of Indigenous Peoples Act (Canada)|United Nations Declaration on the Rights of Indigenous Peoples (UNDRIP)]].<ref>{{Cite web|title=United Nations Declaration on the Rights of Indigenous Peoples {{!}} United Nations For Indigenous Peoples|url=https://www.un.org/development/desa/indigenouspeoples/declaration-on-the-rights-of-indigenous-peoples.html|access-date=2021-09-16|website=www.un.org}}</ref> CARE was created by the International Indigenous Data Sovereignty Interest Group, a group that is a part of the [[Research Data Alliance|Research Data Alliance.]] <ref>{{cite web |last1=Carroll, Stephanie Russo; Garba, Ibrahim; Figueroa-Rodríguez, Oscar L.; Holbrook, Jarita; Lovett, Raymond; Materechera, Simeon; Parsons, Mark; Raseroka, Kay; Rodriguez-Lonebear, Desi; Rowe, Robyn; Sara, Rodrigo; Walker, Jennifer D.; Anderson, Jane; Hudson, Maui |title=The CARE Principles for Indigenous Data Governance |url=https://datascience.codata.org/articles/10.5334/dsj-2020-043/ |website=datascience.codata.org |publisher=Data Science Journal |access-date=9 October 2022}}</ref>
CARE is an acronym which stands for '''C'''ollective Benefit, '''A'''uthority to Control, '''R'''esponsibility, '''E'''thics.<ref>{{Cite web|date=2021-08-27|title=CARE Principles of Indigenous Data Governance — Global Indigenous Data Alliance|url=https://www.gida-global.org/care|access-date=2021-09-16|archive-url=https://web.archive.org/web/20210827235045/https://www.gida-global.org/care|archive-date=2021-08-27}}</ref>
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