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This survey is being conducted by members of the PEPR Partnership – standing for Partnership for the Engagement of People in Pain Research. We are inviting people with lived experience of chronic pain who have been involved in research or engaged in research adjacent organizations, nationally funded research networks, national…
You are being asked to participate because you have lived or living experience (as a patient, caregiver, or health care professional) of heart failure. Your heart and your brain are intimately connected. People with heart failure may experience changes to their brain, their thinking, or their mental health. We call…
Would you like to join a group that works to improve pregnancy and post pregnancy care? Join the GEM Hub! We co-create impactful knowledge mobilization activities to improve pregnancy and post-pregnancy care and help reduce severe maternal morbidity and mortality. Background: Interested patient partners will be encouraged to…
Across Canada, there’s growing momentum to rethink how health data is accessed, shared, and used – and the public needs a strong voice in that future. OurHealthData is a new movement designed to empower and bring Canadians together to understand and shape the responsible use of health data! What…
November 2-8, 2025 is National Pain Awareness Week, a time to raise awareness of chronic pain, its impacts, and how implementing An Action Plan for Pain in Canada can improve equitable access to timely and evidence-based care and support for all people with pain. The plan lays out numerous recommendations…
In recognition of Canadian Patient Safety Week, please join us for a free, 1-hour webinar packed with helpful information and tools for people managing multiple medications. Organized in partnership with the Canadian Medication Appropriateness and Deprescribing Network (CADeN), the Institute for Safe Medication Practices Canada,…
Study goals The overarching goal of our research is to integrate equity in incident reporting and patient complaints systems in Canadian hospitals. Incident reporting and patient complaints systems are structured hospital processes for reporting, analyzing and addressing adverse events and patient concerns and contributing factors. However, these systems are…
University Health Network (UHN) in Toronto is conducting a Quality Improvement Project on Responsible AI: Patient Charter of Rights funded by the Future Skills Centre. This project brings together patients, caregivers, health care professionals, and experts to ensure the health system understands what patients and caregivers expect and trust…
What is this about? Recommendations made by health organizations rest on a scale. On this scale, some recommendations can be “stronger” than others. This “strength” should be easily understood by everyone, including members of the public and health care professionals. The survey results will help us find a better…
We need your help to understand what supports the family caregivers of ICU (Intensive Care Unit) survivors who are discharged home need to support their participation in health research. Are you? • Over the age of 18 years • Living in Canada • A family caregiver to…
Health Quality BC administers the Patient Voices Network. Using evidence-informed strategies, the Council shifts culture, improves clinical practice and advances person- and family-centred care to support high-quality care for every person in our province.
