CARE Principles for Indigenous Data Governance

The CARE Principles for Indigenous Data Governance are a set of principles intended to guide open data projects in engaging Indigenous Peoples rights and interests. CARE was created in 2019 by the International Indigenous Data Sovereignty Interest Group, a group that is a part of the Research Data Alliance.^[1] It outlines collective rights related to open data in the context of the United Nations Declaration on the Rights of Indigenous Peoples and Indigenous data sovereignty. ^[2]

CARE is an acronym which stands for Collective Benefit, Authority to Control, Responsibility, Ethics. The CARE Principles are 'people and purpose-oriented, reflecting the crucial role of data in advancing Indigenous innovation and self-determination', and intended as a complement to the data-oriented perspective of other standards such as FAIR data (findable, accessible, interoperable, reusable).^[3]

The CARE principles have been embedded into the Beta version of Standardised Data on Initiatives (STARDIT).^[4] CARE principles were the basis of a submission to the UN's Global Digital Compact.^[5][6]

See also

• FAIR data
• First Nations principles of OCAP
• Data sovereignty
• Indigenous data governance