NEWS & EVENTS

Indigenous data sovereignty in health research - 16 April

Explore the concept of Indigenous data sovereignty in health research and learn how to apply it through Indigenous data governance.

Event details

Date: Tuesday 16 April 2024

Time: 11am-12pm (AEST-QLD)

Please note that this session will not be recorded. However, session attendees will be provided with a condensed PDF version of the slides for their own personal use after the workshop.

Presenter

  • Neane Carter, Solicitor, Terri Janke and Company.
    Neane is a proud Djaara, Yorta Yorta, Wamba Wamba, Wergaia, Wotjobaluk woman from northern and central Victoria

Additional resources

Indigenous Cultural and Intellectual Property (ICIP) refers to Indigenous peoples’ rights to their cultural heritage, traditional knowledge and traditional cultural expressions. This is enshrined in the United Nations Declaration on the Rights of Indigenous Peoples. Where a research project is being undertaken it is important to consider what ICIP is incorporated, and how ICIP will be protected.

Further resources to assist in your knowledge of best practice engagement with First Nations people and their ICIP, please refer to:

  • UNDRIP Community Guide - assists Aboriginal and Torres Strait Islander people familiarise themselves with UNDRIP and how the rights can be used in everyday life.
  • UNDRIP Business Guide - provides practical guidance for business to understand, respect, support the rights of Aboriginal and Torres Strait Islander people, and embed those rights into business practices.

Further resources to assist in your knowledge and implementation of IDSov and IDGov, please refer to:

For further information about the work of Terri Janke and Company and the 10 True Tracks® principles please refer to the Terri Janke and Company website.

More information

For more information about this workshop please email events@healthtranslationqld.org.au.

HTQ Autumn Seminar Series

This seminar is part of HTQ’s Autumn Seminar Series where we will delve into important topics in health research data management, including governance, planning, documentation, and Indigenous data sovereignty.

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