White paper consultation - List of stakeholder submissions

Canada's commitment to open government is part of the federal government's efforts to foster greater openness and transparency to provide Canadians with more opportunities to learn about and participate in government and, at the same time, create a more efficient and responsive government.

If you would like to receive any of the submissions listed below, please specify which submissions and contact us at: rmod_stakeholders-intervenants_dgro@hc-sc.gc.ca

Stakeholder Submissions
Date received Name Organisation
2017-04-28 Yan Xu, M.D., RCPSC Internal Medicine Resident Department of Medicine, University of Toronto
2017-04-30 Laura King, Head of Regulatory Affairs & Global Drug Development Novartis Pharmaceuticals Canada Inc.
2017-05-14 Michael Kruse, Executive Director Bad Science Watch
2017-05-15 Jamie Scott, MD, PhD Professor & Canada Research Chair, Simon Fraser University
2017-05-17 Kristin Willemsen, Director of Scientific & Regulatory Affairs Consumer Health Products (CHP) Canada
2017-05-17 Angus Campbell individual submission
2017-05-19 Elizabeth Borek individual submission
2017-05-19 Jamie Falk, PharmD, Assistant Professor College of Pharmacy, University of Manitoba
2017-05-19 Anne & Paul Caron individual submission
2017-05-19 Jane Turner, President (sent by Devika Krishnan) REACH Community Health Centre
2017-05-19 Michael Furman University of Cambridge, UK
2017-05-19 Margot Duley individual submission
2017-05-20 Andrée Crépeau, individual submission
2017-05-20

Dr. Joel Lexchin, MD, Professor Emeritus, et.al.

Author's submission undersigned by 120 individual academics, health researchers, health professionals, and/or patient advocates.

School of Health Policy and Management, Faculty of Health, York University

Signatories' organisational affiliation(s) included.

2017-05-20 Jane Macdonald individual submission
2017-05-21 Matt Oxman Informed Health Choices
2017-05-21 John-Jose Nunez, MD University of British Columbia
2017-05-23 Michael West, Professor of Medicine & Assistant Dean Research - Clinical Trials Dalhousie Medical School, Dalhousie University
2017-05-23 Dan Ryder, Associate Professor Irving K. Barber School of Arts and Sciences, University of British Columbia
2017-05-24 Brian Lewis, President & CEO MEDEC
2017-05-24

Janet Currie (PhD Candidate, UBC), et.al.

Author's submission undersigned by 5 individual academics, health researchers, health professionals, and/or patient advocates.

Independent Voices for Safe and Effective Drugs (IVSED)

Signatories' organisational affiliation(s) included.

2017-05-25 Angela Spelsberg Chair, Working Group on Health, Transparency International Germany
2017-05-25 Aled Edwards, Chief Executive Structural Genomics Consortium (SGC)
2017-05-25 Tara Federici, VP - Technology and Regulatory Affairs, AdvaMed (Advanced Medical Technology Association)
2017-05-25 Marleine El-Ghazal (for Keith McIntosh), Innovative Medicines Canada (IMC)
2017-05-25 Anne Wilkie, VP - Scientific & Regulatory Affairs Canadian Generic Pharmaceutical Association (CGPA)
2017-05-25 Katie Gibbs, Executive Director Evidence for Democracy
2017-05-25 Sarah Jennings, Acting Manager, Professional and Regulatory Affairs National Association of Pharmacy Regulatory Authorities (NAPRA)
2017-05-25 Rikesh Gandhi, Manager, Regulatory Affairs (on behalf of: Christopher Fredric, Associate Director, Regulatory Affairs) Alexion Pharma Canada
2017-05-25 Maggy Mouradian, Established Products & Regulatory Operations Manager Boehringer Ingelheim (Canada) Ltd.
2017-05-26 Margaret E. McCarthy, Executive Director, Collaboration for Research Integrity and Transparency (CRIT), Yale Law School
2017-05-26 Donald Elrick, Director Regulatory Affairs, Immunology Janssen Inc.
2017-05-26 Lesia Babiak, Executive Director, Worldwide Government Affairs & Policy (Canada) Johnson & Johnson
2017-05-26 Sally Prawdzik, Director, Regulatory Policy Innovation Johnson & Johnson
2017-05-26 Corina Voda, Regulatory Affairs Project Manager AbbVie Corporation
2017-06-09 (originally submitted: 2017-05-26) Terence Young, Chair Drug Safety Canada
2017-05-26 Rocelyn DelCarmen, Director, Regulatory Affairs and Quality Assurance AstraZeneca Canada Inc.
2017-05-26 Kevin Anderson (on behalf of Dr. Khaled El Emam) Pharmaceutical Users Software Exchange (PhUSE),
2017-05-26 Stephanie Croley, Regulatory Affairs Specialist Purdue Pharma (Canada)
2017-05-26 Leslie Holt individual submission
2017-05-26 Sandra Wainwright, Executive Director, Regulatory Affairs Merck Canada Inc.
2017-05-26 Andrew Casey, President & CEO, with comments from Ron Boch BIOTECanada
2017-05-26 Arshia Ghani, Associate Director, Regulatory Affairs Pfizer Canada Inc.
2017-05-26 Khaled El Emam, President, & Hazel Nicholls Privacy Analytics
2017-05-31 Sylvie Leblanc individual submission

Learn about how Health Canada will handle information from meetings and correspondence with stakeholders related to implementation of its proposal for public release of clinical information in drug submissions and medical device applications.

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