Speaker Presentations - Day One
From Evidence to Policy to Practice
Monday, April 3, 2006
Processes and mechanisms for contextualizing scientific evidence – Moving from HTA to HTPA?
- Véronique Déry, Chief Executive Officer and Scientific Director, AETMIS
- Ron Goeree, Jim Bowen, Jean-Eric Tarride, Gord Blackhouse, Daria O’Reilly, Rob Hopkins
- Chris McCutcheon, Senior Program Officer, Canadian Health Services Research Foundation
The Use of Recommendations in Decision Making: A Multi-Dimensional Perspective
- Dr Marie-Pierre Gagnon, Université Laval
Linking Evidence & Policy: The Alberta Model
- Henry Borowski, Director, Health Technologies & Services Policy, Alberta Health and Wellness
- Kirsten Garces, Manager CETAP/HTIS – Pharmaceuticals, CADTH
Enhancing HTA Use in Low-Resource Jurisdictions
- Dr. Stephen Bornstein, Director, Newfoundland and Labrador Centre for Applied Health Research
- Sheila Tucker, CADTH Liaison Officer for Newfoundland & Labrador
Expensive Drugs for Rare Diseases: Experience at the decision making Front
- Dr. Janet Martin, Director, High Impact Technology Evaluation Centre, London Health Sciences Centre
Drug class reviews and formulary management: a survey of Canadian jurisdictions
- Michel Boucher, Research Officer, CADTH
PHAC / CACDS Point-Of-Sale (Pos) Data Sharing Initiative
- Allan Malek, Vice President, Pharmacy, Canadian Association of Chain Drug Stores
- Victoria L. Edge, BSc., MSc., PhD Candidate, Epidemiologist Foodborne, Waterborne & Zoonotic Infections Division, Public Health Agency of Canada
Pharmaceutical Benefit Plans for Children: Using Evidence to Improve Outcomes
- Dr. Wendy Ungar, Scientist, Hospital for Sick Children
Synthesizing evidence on the front line: Can it work?
- Sarah Hayward, CEO, SEARCH Canada
- Rhona McGlasson, Total Joint Network
- Dr. Karmela Krleza-Jeric, CIHR
Parameters of Success in Decision Making
- Shannon Madden, University of Toronto
Litigating Access to Health Care Services in Canada: The Role of HTA in the Courtroom
- Nola Ries, Research Associate, Health Law Institute, University of Alberta
Implicit Health Technology Assessment: A Descriptive Study of Ontario Appeal Board Cases
- Mita Giacomini, McMaster University
Cumulative Meta-Analysis to Determine Key Milestones in the Life Cycle of Evidence in Cancer Care
- Dr. Neil Reaume, Ottawa Health Research Institute/The Ottawa Hospital Regional Cancer Centre
Hospital HTPA: Mandate or Wishful Thinking?
- Dr. Janet Martin, Director, High Impact Technology Evaluation Centre, London Health Sciences Centre
- Dr. Marie-Pierre Gagnon, Université Laval
- Arjun C. Rao, Senior Project Specialist, Clinical Technology Assessment and Innovation Decision Support and Quality Management Unit, Massachusetts General Hospital
Evidence-based recommendations – Is it “just evidence” or “beyond evidence”?
- Karen Lee, Health Economist, CDR, CADTH (Convenor)
Panelists:
- Dr. Andreas Laupacis, President and CEO, Institute for Clinical Evaluative Sciences
- Dr. Terri O’Grady, Clinical Reviewer, Common Drug Review Director, CADTH
- Dr. Reiner Banken, Deputy Chief Executive Officer, Development and Partnerships, AETMIS
- Bob Nakagawa, Assistant Deputy Minister, Pharmacare, BC Ministry of Health
- Dr. Dawn Stacey, Assistant Professor, School of Nursing, University of Ottawa
Consumer Involvement in Decision Making for Health Care Policy and Planning
- Nancy Santesso, Knowledge Translation Specialist, Cochrane Musculosketetal Group
- Anne Dooley, President, Canadian Arthritis Patient Alliance
Linking the public in priority-setting for HTA: Findings from a citizen’s jury
- Tania Stafinski, University of Alberta
- Dr. Devidas Menon, Professor Health Policy and Management Program, University of Alberta