Rendre évident : une approche symétrique de la réglementation des produits thérapeutiques
Author:
Affiliation:
1. Department of Bioethics, Dalhousie University, 5849 University Ave, Halifax, Nouvelle-Écosse, Canada B3H 4H7
2. Technoscience and Regulation Research Unit, Dalhousie University, 5849 University Ave, Halifax, Nouvelle-Écosse, Canada B3H 4H7
Abstract
Publisher
Consortium Erudit
Subject
General Earth and Planetary Sciences,General Environmental Science
Reference89 articles.
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3. Abraham, J. et H. L. Smith (2003), Regulation of the Pharmaceutical Industry, New York, Palgrave Macmillan.
4. Abraham, J. et C. Davis (2009), « Drug Evaluation and the Permissive Principle : Continuities and Contradictions between Standards and Practices in Antidepressant Regulation », Social Studies of Science, vol. 39, no 4, p. 569-598.
5. Abramson, J. et B. Starfield (2005), « The Effect of Conflict of Interest on Biomedical Research and Clinical Practice Guidelines : Can We Trust the Evidence in Evidence-Based Medicine ? », Journal of the American Board of Family Practice, vol. 18, no 5, p. 414-418.
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