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CARE Principles for Indigenous Data Governance

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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 (UNDRIP).[1]

CARE is an acronym which stands for Collective Benefit, Authority to Control, Responsibility, Ethics.[2]

While CARE can be considered part of the open data movement, it aims to build on other standards such as FAIR (findable, accessible, interoperable, reusable) by considering power differentials and historical contexts. The CARE Principles for Indigenous Data Governance are 'people and purpose-oriented, reflecting the crucial role of data in advancing Indigenous innovation and self-determination'.[3]

The CARE principles have been embedded into the Beta version of Standardised Data on Initiatives.[4][5]

References

  1. ^ "United Nations Declaration on the Rights of Indigenous Peoples | United Nations For Indigenous Peoples". www.un.org. Retrieved 2021-09-16.
  2. ^ "CARE Principles of Indigenous Data Governance — Global Indigenous Data Alliance". web.archive.org. 2021-08-27. Retrieved 2021-09-16.
  3. ^ "Who We Are — Global Indigenous Data Alliance". web.archive.org. 2021-09-16. Retrieved 2021-09-16.
  4. ^ "Standardised Data on Initiatives – STARDIT: Beta Version". osf.io. doi:10.31219/osf.io/w5xj6. Retrieved 2021-09-16.{{cite web}}: CS1 maint: url-status (link)
  5. ^ "Beta - Science For All". web.archive.org. 2021-09-16. Retrieved 2021-09-16.
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