The generic Informed Consent Service gICS(®): implementation and benefits of a modular consent software tool to master the challenge of electronic consent management in research

BACKGROUND: Defining and protecting participants’ rights is the aim of several ethical codices and legal regulations. According to these regulations, the Informed Consent (IC) is an inevitable element of research with human subjects. In the era of “big data medicine”, aspects of IC become even more...

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Detalles Bibliográficos
Autores principales: Rau, Henriette, Geidel, Lars, Bialke, Martin, Blumentritt, Arne, Langanke, Martin, Liedtke, Wenke, Pasewald, Sandra, Stahl, Dana, Bahls, Thomas, Maier, Christian, Prokosch, Hans-Ulrich, Hoffmann, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391490/
https://www.ncbi.nlm.nih.gov/pubmed/32727514
http://dx.doi.org/10.1186/s12967-020-02457-y

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