This article outlines the creation of a research governance model aimed at reviewing and approving diabetes research projects with a focus on ethical standards and patient engagement. The model ensures that research projects align with the needs and priorities of the community. Diabetes Action Canada played a crucial role in the development of this governance framework by involving diverse stakeholders, including patients and researchers.
Episode six features Kylie Peacock, a Diabetes Action Canada Patient Partner and Conrad Pow, a Senior Project Manager at Diabetes Action Canada discussing the National Diabetes Repository and how Diabetes Action Canada is using data to change lives.
Episode four discusses how we can use data to improve health care. Guests Devin Cleary and Dr. Alanna Weisman discuss their research projects in this area – in particular how they are trying to improve outcomes for people with type 1 diabetes.
National data repository now available to diabetes researchers This week, Diabetes Research Connect, a national, virtual data repository, launched. The data repository, a collaboration between Diabetes Action Canada and the Canadian Primary Care Sentinel Surveillance Network (CPCSSN), aims to enhance diabetes research across Canada and foster partnerships with academic institutions, healthcare providers and patient groups. […]