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Collective interests, health research ethics and data governance for Indigenous Sámi populations

by Susanna Ragnhild Andersdatter Siri, Christina Storm Mienna, Per Axelsson The General Data Protection Regulation (GDPR) provides a robust framework for regulating individual data collection, use, reuse, and storage across Europe, but offers limited safeguards for collective rights, such as those of Indigenous peoples. Here, we examine specific ethical guidelines and governance principles…

We haven't written up this one. PLOS Medicine has the full story — the link below goes straight to it.

Read the original at journals.plos.org →

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