Research priorities

Systemic racism has created barriers and inequity in government services. To address this, we need to know where it’s happening and who’s affected. The Anti-Racism Data Act is giving us the tools we need to look into these issues.
Under the Anti-Racism Data Act, we’re required to set research priorities every two years. This page outlines the current research priorities and how they were developed. These priorities are meant to help steer government towards research that identifies systemic barriers and requires action to advance racial equity.
We develop research priorities through consultation and cooperation with Indigenous Peoples and in collaboration with the Anti-Racism Data Committee. Setting priorities in this way helps to focus our research on the areas that matter most to Indigenous Peoples and racialized communities.
Some priorities may be in areas where government lacks data or where data collection is limited to avoid community harm. By naming them as priorities we’re able to investigate gaps in information and barriers to accessing information, and support program areas to fill those gaps safely.
Our work on research priorities builds upon existing research and recommendations (for example, the In Plain Sight report, which focuses on anti-Indigenous racism in health care), and helps us understand the legacy of colonial policies in B.C. Research is guided by a distinctions-based approach to Indigenous data sovereignty and self-determination and other important process commitments.
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Research Priorities 2025-2027
On May 30, 2025, we published research priorities for 2025-2027.
To create these priorities, Indigenous Peoples and the Anti-Racism Data Committee reflected on feedback, reports and recommendations gathered from partners, community members and advocates over the last few years.
Many research priorities for 2025-2027 build upon previous priorities and calls to action. This reflects the persistent and pressing nature of these issues and their historical and continued impact on racialized communities and the rights and interests of Indigenous Peoples in B.C.

Research Priorities from Indigenous Peoples
The 2025-2027 research priorities reflect the common themes we heard from Indigenous Peoples who participated in the consultation and cooperation process. They do not reflect all of the distinct and unique issues of systemic racism facing First Nations, Métis and Inuit people across B.C.
Research Priorities from the Anti-Racism Data Committee
The Anti-Racism Data Committee recommended nine priorities for 2025-2027. Seven of these build upon the previous priorities while two are new areas of research.

Thank you
Setting research priorities takes considerable time and effort. Reflecting on experiences of racism can be challenging and this work takes an emotional toll. We’re grateful to the partners and individuals who contributed and for their willingness to share and trust us with their recommendations.
With their thoughtful input, we’ve created a list of priorities that reflects the interests of Indigenous and racialized communities and will help to drive research across government. This list is a key part of our ongoing efforts to identify and address systemic racism and advance racial equity over the coming years.
How will research be conducted?
Under the Anti-Racism Data Act, we aim to increase trust, transparency and accountability. At the same time, it’s important to prevent and reduce harms to Indigenous Peoples and racialized communities.
We collaborated with the Anti-Racism Data Committee and Indigenous Peoples to develop five process commitments. These commitments will apply to each research project conducted under the Act.
Indigenous data sovereignty
Guided by a distinctions-based approach to Indigenous data sovereignty and self-determination.


Data justice
Data justice recognizes both the harm that data has caused communities, as well as the power of data to advance equity and social justice.
Intersectionality
An individual may experience more than one form of discrimination and/or marginalization.
Research must consider a person’s whole identity while maintaining an anti-racism and gender-based lens.


Transparency
To build trust, we must be clear about the purpose and benefit of data collection.
This means working with communities to understand how and when to share data, methodologies, and findings.
Continuing involvement
We’ll continue to build and strengthen relationships with communities and partners.
This will ensure that the needs, experience and knowledge of Indigenous Peoples and other racialized individuals guide data collection and research.
