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IRB|August 9, 2018
Recontacting Pediatric Research Participants for Consent When They Reach the Age of MajorityBartha Maria Knoppers, Karine Sénécal, Joanne Boisjoli, et al.
Frontiers in Medicine|June 13, 2022
Digitizing the Informed Consent Process: A Review of the Regulatory Landscape in the European UnionEvelien De Sutter, Janos Meszaros, Pascal Borry, et al.
Journal of Empirical Research on Human Research Ethics : JERHRE|July 7, 2016
Participants' Accounts on Their Decision to Join a Cohort Study With an Attached Biobank: A Qualitative Content Analysis Study Within Two German StudiesHélène Nobile, Manuela M Bergmann, Jennifer Moldenhauer, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|December 20, 2008
Donation after uncontrolled cardiac death (uDCD): a review of the debate from a European perspectivePascal Borry, Walter Van Reusel, Leo Roels, et al.
Critical Reviews in Clinical Laboratory Sciences|January 31, 2017
Unsolved challenges in pediatric whole-exome sequencing: A literature analysisGabrielle Bertier, Karine Sénécal, Pascal Borry, et al.
Journal of Community Genetics|October 12, 2012
The challenge of implementing genetic tests with clinical utility while avoiding unsound applicationsMartina C Cornel, Carla G van El, Pascal Borry
Human Mutation|September 21, 2016
Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing CompaniesEmilia Niemiec, Pascal Borry, Wim Pinxten, et al.
BMC Health Services Research|February 22, 2023
Informing a European guidance framework on electronic informed consent in clinical research: a qualitative studyEvelien De Sutter, Pascal Borry, Isabelle Huys, et al.
BMC Medical Ethics|August 1, 2021
Personalized and long-term electronic informed consent in clinical research: stakeholder viewsEvelien De Sutter, Pascal Borry, David Geerts, et al.
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