Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Rosemarie D L C Bernabe"'
Autor:
Karen Stendal, Rosemarie D L C Bernabe
Publikováno v:
Journal of Medical Internet Research, Vol 26, p e41670 (2024)
Since the introduction of virtual environments in the 70s, technologies have moved through virtual reality, mixed reality, and augmented reality into extended reality (XR). This development is promising for various groups. Previous research has shown
Externí odkaz:
https://doaj.org/article/20c9c439eb354bc89c726cff0f652812
Autor:
Rosemarie D. L. C. Bernabe, Ghislaine J. M. W. van Thiel, Nancy S. Breekveldt, Christine C. Gispen, Johannes J. M. van Delden
Publikováno v:
BMC Medical Ethics, Vol 21, Iss 1, Pp 1-8 (2020)
Abstract Background In the EU, clinical assessors, rapporteurs and the Committee for Medicinal Products for Human Use are obliged to assess the ethical aspects of a clinical development program and include major ethical flaws in the marketing authori
Externí odkaz:
https://doaj.org/article/39b586aa966944d7bde67fb0fc8bd504
Autor:
Yemisrach Zewdie Seralegne, Cynthia Khamala Wangamati, Rosemarie D. L. C. Bernabe, Bobbie Farsides, Abraham Aseffa, Martha Zewdie
Publikováno v:
Developing world bioethics.
Few studies in sub-Saharan Africa evaluate Institutional Review Boards (IRBs) capacity. The study aims to explore the composition of IRBs, training, and challenges experienced in the ethics review processes by members of research institutions and uni
Publikováno v:
Current medical research and opinion. 37(6)
To conduct a descriptive content analysis of normative documents on the role of research ethics committees (RECs) after the approval of clinical trial protocols. The question to be addressed is whether and to what extent normative documents support a
Autor:
Bjørn Hofmann, Søren Holm, Anne Kari Tolo Heggestad, Heidi Beate Bentzen, Reidar Pedersen, Anne Hambro Alnaes, Shereen Cox, Annette Robertsen, Jan Helge Solbakk, Rosemarie D. L. C. Bernabe
Publikováno v:
Solbakk, J H, Bentzen, H B, Holm, S, Heggestad, A K T, Hofmann, B, Robertsen, A, Alnæs, A H, Cox, S, Pedersen, R & Bernabe, R 2020, ' Back to WHAT? The role of research ethics in pandemic times ', Medicine, Health Care and Philosophy . https://doi.org/10.1007/s11019-020-09984-x
Medicine, Health Care and Philosophy
Medicine, Health Care, and Philosophy
Medicine, Health Care and Philosophy
Medicine, Health Care, and Philosophy
The Covid-19 pandemic creates an unprecedented threatening situation worldwide with an urgent need for critical reflection and new knowledge production, but also a need for imminent action despite prevailing knowledge gaps and multilevel uncertainty.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15c41b9921c7bc311099adf152c29034
https://doi.org/10.1007/s11019-020-09984-x
https://doi.org/10.1007/s11019-020-09984-x
Autor:
G. J. M. W. van Thiel, Rosemarie D. L. C. Bernabe, J.J.M. van Delden, Christine C. Gispen, Nancy S. Breekveldt
Publikováno v:
Drug Discovery Today. 23:205-207
Publikováno v:
Current medical research and opinion. 35(11)
Objectives: Ethics guidelines such as the Declaration of Helsinki and the CIOMS International Ethical Guidelines for Health-related Research Involving Humans require the sponsors, in cooperation with relevant stakeholders, to provide post-trial acces
Autor:
Christine C. Gispen, Johannes J. M. van Delden, Rosemarie D. L. C. Bernabe, Nancy S. Breekveldt, Ghislaine J. M. W. van Thiel
Publikováno v:
BMC Medical Ethics
BMC Medical Ethics, Vol 21, Iss 1, Pp 1-8 (2020)
BMC Medical Ethics, Vol 21, Iss 1, Pp 1-8 (2020)
Background In the EU, clinical assessors, rapporteurs and the Committee for Medicinal Products for Human Use are obliged to assess the ethical aspects of a clinical development program and include major ethical flaws in the marketing authorization de
Autor:
G. J. M. W. van Thiel, C. C. Gispen-de Wied, J.J.M. van Delden, Nancy S. Breekveldt, Rosemarie D. L. C. Bernabe
Publikováno v:
Current Medical Research and Opinion, 35(4), 637. Informa Healthcare
Background: Within the EU, regulators are obliged to take ethical issues into consideration during marketing authorization deliberation. The goal of this manuscript is to identify what kinds of ethical issues regulators encounter during marketing aut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ec42513f73c1822ac768e5c22dcff3e
https://dspace.library.uu.nl/handle/1874/381166
https://dspace.library.uu.nl/handle/1874/381166
Publikováno v:
British Journal of Clinical Pharmacology. 78:1248-1256
In the European Medicines Agency (EMA), the involvement of patients has been increasingly recognized as valuable and necessary. Specifically in scientific committees, patients through patient representatives are actively involved in deliberations and