Consent for access to health data for research.
Accessing the right data, at the right place and time—with patients’ consent.
The GRIIS research team brings together professionals in computer science, medicine, health care and social services, law, ethics and philosophy.
The GRIIS interdisciplinary projects address critical issues — from IT and informatics to health care systems, from clinical practice to biomedical research, from law to ethics.
Society is becoming more complex. Health data is stored in many different places. Researchers and clinicians need access to this data to deliver patient-centred health care. This data is also needed to improve the quality, cost and efficiency of health care services.
What if clinicians could integrate new knowledge seamlessly into their practice?
The GRIIS conducts research that helps health systems improve health care. Quality health care is:
The health care system must avoid harming patients.
Health care should be evidence-based.
Clinicians should make their decisions taking into account patients’ biology, culture and sociocultural context.
Unnecessary delays suggest defects in the system of health care.
A system should minimize the loss of resources, funds, opportunities, time, space, capital and ideas.
Gender, ethnicity and income should not deprive patients of the best possible health care.
Consent for access to health data for research.
Accessing the right data, at the right place and time—with patients’ consent.
GRIIS researchers publish articles in computer science, informatics, law, ethics and philosophy.
Groupe de recherche interdisciplinaire en informatique de la santé
Université de Sherbrooke
2500, boul. de l'Université, Sherbrooke (Québec) J1K 2R1 Canada
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