基本説明
Proposes a uniquely Canadian framework for striking a balance between the benefits of allowing researchers to access medical information and the privacy concerns of individuals.
Full Description
Proposes a framework for striking a balance between the benefits of allowing researchers to access medical information and the privacy concerns of individuals
Contents
Contributors include Wendy Armstrong (Consumers' Association of Canada, Alberta), Penny Ballem (Consultant), David Henry (Institute for Clinical Evaluative Sciences), Alan Katz (Manitoba Centre for Health Policy), Pat Kosseim (Genome Canada), Shoo Lee (Mount Sinai Hospital, Toronto), Steven Lewis (Consultant), Lisa Lix (University of Saskatchewan), William Lowrance (Consultant), Pat Martens (Manitoba Centre for Health Policy), Dale McMurchy (Consultant), Andrew F. Nelson (Health Partners Research Foundation), Robert Ouellet (Canadian Medical Association), Dorothy Pringle (University of Toronto), Robert J. Reid (Group Health Centre for Health Studies), Valerie Steeves (University of Ottawa), Terry Sullivan (Cancer Care Ontario), Simon Sutcliffe (British Columbia Cancer Agency), Robyn Tamblyn (McGill University), Jack Tu (Institute for Clinical Evaluative Studies), Don Willison (McMaster University), Michael Wolfson (Statistics Canada), and Glenda Yeates (Canadian Institute for Health Information).
