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Data Data Everywhere
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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).

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Proposes a framework for striking a balance between the benefits of allowing researchers to access medical information and the privacy concerns of individuals

About the Author

Colleen M. Flood is a Canada Research Chair at the Faculty of Law, University of Toronto. From 2006-2011 she served as the Scientific Director of the Canadian Institute for Health Services and Policy Research."

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