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 r...

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Bibliographic Details
Published in:	Journal of translational medicine Vol. 18; no. 1; pp. 287 - 12
Main Authors:	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
Format:	Journal Article
Language:	English
Published:	London BioMed Central 29.07.2020 BioMed Central Ltd Springer Nature B.V BMC
Subjects:	Automation Biomedical and Life Sciences Biomedicine Computer programs Consent management Data collection Disease management Electronic health records Electronics Ethical aspects Ethics GDPR General data protection regulation Human subjects Humans Informed Consent Laws, regulations and rules Medical research Medicine/Public Health Open source software Personal health Research Design Research Personnel Software Software industry Translational Medicines ‘Ecosystem’ Informed consent Consent management General data protection regulation GDPR
ISSN:	1479-5876, 1479-5876
Online Access:	Get full text
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