Health Data for All of Us – Past Events
Look below for information on our past events in this series…
![No significant visuals. A word cloud banner on the left side and HDRN Canada watermark map logo at the bottom right. Text reads: Health Data for All of Us 2023: earning trust and transparency.](https://cdp.hdrn.ca/wp-content/themes/hdrn-canada/library/images/blank.gif)
Health Data for All of Us: Earning Trust through Transparency
HDRN Canada’s second public forum took place in Montreal and…
![No significant visuals. A word cloud banner on the left side and HDRN Canada watermark map logo at the bottom right. Text reads: Health Data for All of Us 2023: sharing ideas and priorities](https://cdp.hdrn.ca/wp-content/themes/hdrn-canada/library/images/blank.gif)
Health Data for All of Us: Sharing Ideas & Priorities
HDRN Canada hosted its inaugural public forum in Winnipeg and…
![No significant visuals. A word cloud banner on the left side and HDRN Canada watermark map logo at the bottom right. Text reads: Health Data for All of Us 2023: earning trust and transparency.](https://cdp.hdrn.ca/wp-content/themes/hdrn-canada/library/images/blank.gif)
Health Data for All of Us: Earning Trust through Transparency
HDRN Canada’s second public forum took place in Montreal and online in 2024. Speakers explored the importance, necessity and complexity of building and maintaining public trust in health data access and use, highlighting the need for patient-centred data practices, the inclusion of sex and gender in data, ongoing engagement with public partners, and respect for Indigenous data sovereignty.
![No significant visuals. A word cloud banner on the left side and HDRN Canada watermark map logo at the bottom right. Text reads: Health Data for All of Us 2023: sharing ideas and priorities](https://cdp.hdrn.ca/wp-content/themes/hdrn-canada/library/images/blank.gif)
Health Data for All of Us: Sharing Ideas & Priorities
HDRN Canada hosted its inaugural public forum in Winnipeg and online in 2023 to generate dialogue among members of the public, researchers and other stakeholders about their priorities for and challenges to data-intensive health research. Discussion topics focused on the importance of public input into health data collection, sharing and use, with overarching themes of inclusion, diversity, equity and accessibility.