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Ninth International Conference on Clinical Ethics Consultation (ICCEC), Munich, Germany, March 2013The Ninth International Conference on Clinical Ethics Consultation (ICCEC) 2013 will take place in Munich, Germany in March 2013. It is dedicated to the motto "Clinical ethics: bridging clinical medicine and ethics". The aim is to bring together ethicists, ethics consultants, and clinicians to reflect on their related practices, needs, concepts, and research results. We encourage you and all colleagues who are interested in these discussions to submit their abstracts to the conference - deadline is October 15th. If you have any questions or need for further information please visit our website http://www.iccec2013.de/call-for-abstracts/abstract-guidelines/abstract-guidelines.html or contact us directly via info@iccec2013.de.
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Bookmarked by Dina Bogecho on 20 Sep 2012
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PLOS Medicine: Misrepresentation of Randomized Controlled Trials in Press Releases and News CoverageThis article reports on levels of spin - intentional or unintentional emphasis on the beneficial effect of the experimental treatment - in research abstracts and press releases.
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Bookmarked by Susan Bull on 19 Sep 2012
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Institutional Review BlogIn this frequently updated blog Zachary M. Schrag critically disusses a number of issues relevant to the ethical review of humanities and social science research.
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Bookmarked by Susan Bull on 19 Sep 2012
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West African Bioethics Training Program (WABTP) September 2012 Newsletter. Volume 6, Issue 3This edition features the new WABTP website and its characteristics, as well as trainings and activities facilitated, organized and or attended by WABTP members.
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Bookmarked by Stella Adegbehingbe on 17 Sep 2012
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Ethical Considerations in Studying Drug Safety — The Institute of Medicine ReportThe tumult arising from revelations of serious safety risks associated with widely prescribed drugs, including rosiglitazone (Avandia, GlaxoSmithKline), rofecoxib (Vioxx, Merck), and celecoxib (Celebrex, Pfizer), has led to widespread recognition that improvement is needed in our national system of ensuring drug safety. Notwithstanding federal legislation in 2007 that strengthened the authority of the Food and Drug Administration (FDA) in the postmarketing period, critical weaknesses in the national system persist. For the full report see: http://www.nejm.org/doi/full/10.1056/NEJMhle1207160
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Bookmarked by Dina Bogecho on 17 Sep 2012
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